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Journal articles on the topic 'Congenital anomally'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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1

Peter AI, Ekong MB, Ekanem TB, et al. "Attitude and knowledge of pregnant women attending antenatal clinic at St. Luke's Hospital, Anua in Uyo, Nigeria towards congenital anomalies." Ibom Medical Journal 6, no. 2 (2013): 34–40. http://dx.doi.org/10.61386/imj.v6i2.109.

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Context: The birth of a congenitally abnormal child is an event that affects all the family members, and both their internal and external relationships.Objective: To know the attitude and knowledge of women visiting an antenatal clinic in Uyo, Nigeria on congenital anomaly.Study Design: This study was a descriptive cross-sectional study using structured questionnaire with a sample population consisting of 600 pregnant women attending antenatal clinic at St Luke's Hospital, Anua in Uyo, Nigeria.Results: The attitude of respondents towards children with birth defect was that of pity, 286 (47.7%)

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2

Zeynep, Özözen Ayas, and Kotan Dilcan. "A case with Chiari malformation 2 diagnosed with vertigo." Open Journal of Otolaryngology and Rhinology 1, no. 1 (2019): 13–14. https://doi.org/10.36811/ojor.2019.110003.

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Introduction Chiari malformations (CM) are a congenital anomally which posterior fossa structures are displaced from foroman magnum to the upper cervical spinal canal at different degrees [1]. (1) If there is accompanied by spinal dysraphism, it is defined as type 2. Symptoms occurs as a results of pressure on the cerebellum like as vertigo, ataxia, vision problems, headache. In some cases, medical therapy can be used to manage symptoms. Surgery is only treatment for decrease compression or stop progression. This malformation is frequently accompanied by syringomyelia, cystic spaces occur vert

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3

Gupteswar, Mishra, Kumar Rajsamant Nagendra, Kumar Mohanty Sujit, and Das Sankarsan. "Gestational Diabetes Mellitus, its Causes and it's Maternal and Fetal Effect, A Retrospective Study in a Tertiary Care Hospital." International Journal of Current Pharmaceutical Review and Research 15, no. 11 (2023): 682–90. https://doi.org/10.5281/zenodo.11612283.

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AbstractBackground: various degrees ofabnormalities in glucose tolerance during pregnancy detected for the first timeis known as GDM. Global prevalence of GDM is gradually increasing, particularly in developing countries suchas India, where GDM has become one of the major chronic diseases endangering women's health. Poorglycemic control during pregnancy not only harms the mother but also the new born.Methods: A retrospective analysis of pregnant women, specifically those who gave birth in an obstetric ward ofHi-tech medical college and hospital, Bhubaneswar, was performed in this article. A ca

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4

Gupteswar, Mishra1, Kumar Rajsaman Nagendra, Kumar Mohanty Sujit, and Narayan Sahu Aditya. "Pregnancy Complications Associated with Gestational Diabetes Mellitus and Its Causes." International Journal of Current Pharmaceutical Review and Research 15, no. 12 (2023): 291–99. https://doi.org/10.5281/zenodo.11382803.

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Background: GDM is the first occurrence or discovery of various degrees of glucose tolerance abnormalitiesduring pregnancy. Global prevalence of GDM is increasing year by year as society, the economy, and livingstandards improve, particularly in developing countries such as India, where GDM has become one of the majorchronic diseases endangering women's health. Poor blood sugar control during pregnancy not only harms themother but also the new born.Methods: A retrospective analysis of pregnant women, specifically those who gave birth in an obstetric ward ofa tertiary hospital, was performed in

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5

Kratter, Alessandro, Lorenzo Niro, and Corinna Bergamini. "Il quadrifoglio non è sempre sinonimo di fortuna. Un caso di valvola aortica quadricuspide e revisione della letteratura." Cardiologia Ambulatoriale 30, no. 4 (2023): 243–47. http://dx.doi.org/10.17473/1971-6818-2022-4-7.

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Riportiamo un raro caso di anomalia valvolare congenita. Una donna asintomatica di 17 anni è stata indirizzata al nostro laboratorio di ecocardiografia per una valutazione di idoneità allo sport agonistico (pattinaggio artistico). La paziente non presentava altre anomalie cardiache congenite né anamnesi familiare di malattie cardiovascolari. L’ecocardiografia transtoracica e la risonanza magnetica cardiaca hanno rivelato una malformazione quadricuspide della valvola aortica con un lieve rigurgito aortico.

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6

Abdelbaki, Mourad, Wahib Bourida, A. Boureghda, and Roudoci . "Systemic Venous Return Abnormality Associated with An Abnormality of Total Pulmonary Venous Return." Clinical Medicine And Health Research Journal 3, no. 5 (2023): 608–10. http://dx.doi.org/10.18535/cmhrj.v3i5.261.

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This is a 9-year-old child hospitalized for an intraoperative partial venous return anomaly and after an exploration we found a complex congenital cardiac pathology such as an anomaly of total venous return associated with an anomaly of systemic venous return which is mainly seen at early ages Mots-clés Anomalie de retour veineux systémique, Anomalie de retour veineux pulmonaire total, Collecteur Confluence pulmonaire, Urgence néonatale

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7

Hongsakul, Keerati, and Ruedeekorn Suwannanon. "Congenital Absence of Left Circumflex Artery Detected by Computed Tomography Coronary Angiography: A Case Report." Case Reports in Vascular Medicine 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/204657.

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The congenital absence of the left circumflex artery (LCx) is a very rare congenital anomaly of coronary arteries, but it is benign. Currently, the best modality for the diagnosis of coronary anomalies is computed tomography coronary angiography (CTCA). We report a case of congenitally absent LCx with an atypical chest pain.

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8

Jain, Kanika. "A Rare Congenital Anomaly: Jejunal Duplication Cyst." Recent Advances in Pathology & Laboratory Medicine 05, no. 02 (2019): 27–30. http://dx.doi.org/10.24321/2454.8642.201911.

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9

Panesar, G., and V. K. Garg. "Aplasia Cutis Congenita – Case report of a rare case." CARDIOMETRY, no. 25 (February 14, 2023): 1212–14. http://dx.doi.org/10.18137/cardiometry.2022.25.12121214.

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Aplasia cutis congenita (ACC) is a rare malformation characterized by localized congenital absence of the skin. This condition was first described by Cordon in 1767. We present a 2 month old female who presented to Dermatology OPD of Santosh deemed to be University with a scalp defect and diagnosed as Aplasia Cutis Congenita of scalp and no other accompanying anomaly. This case is presented to highlight the importance of recognising the condition.

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10

Pelter, Michele M., Teri M. Kozik, Salah S. Al-Zaiti, and Mary G. Carey. "Congenital Anomaly." American Journal of Critical Care 21, no. 2 (2012): 131–32. http://dx.doi.org/10.4037/ajcc2012505.

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11

Dewan, Pooja, and Rajat Thawani. "Congenital anomaly." Journal of Paediatrics and Child Health 51, no. 7 (2015): 739. http://dx.doi.org/10.1111/jpc.12581.

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12

Al-Saadi, Hatem, Sona Singh, Kanagaraj Marimuthu, et al. "Ultrasound Guided Laparoscopic Port Placement in a Patient with Congenital Anomaly of IVC Undergoing Sleeve Gastrectomy." Obesity Surgery 30, no. 3 (2020): 1168–70. http://dx.doi.org/10.1007/s11695-019-04379-1.

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AbstractWe report a patient with obesity who underwent laparoscopic sleeve gastrectomy after pre-operative ultrasound mark up to enable safe port insertion due to presence of venous collaterals in the abdominal wall as a result of congenial IVC anomaly. This patient was falsely presumed to have NASH cirrhosis. Detailed preoperative workup ruled this out and led to the discovery of congenital IVC anomaly as the cause of engorged blood vessels in the anterior abdominal wall. On table ultrasound mark up of safe sites for port insertion enabled a safe laparosocpic sleeve gastrectomy on this patien

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13

Eguino, Marceo Rodrigo, Adrián Hrabar, and Ernesto Torresani. "ANOMALIA CONGENITA DE ARTERIA CORONARIA IZQUIERDA." Revista Argentina de Cardiología 81, no. 5 (2013): 439. http://dx.doi.org/10.7775/rac.es.v81.i5.3042.

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14

Eguino, Marcelo Rodrigo, Adrián Hrabar, and Ernesto Torresani. "Congenital Anomaly of the Left Coronary Artery." Revista Argentina de Cardiología 81, no. 5 (2013): 413. http://dx.doi.org/10.7775/rac.v81.i5.3042.

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15

Alexis, Emir Noguera Echeverría, Fernanda Ibarra Guerrero María, Gerardo Martínez Morales Mauricio, et al. "Meckel's Diverticulum: A Literature Review of Basic Concepts, Diagnosis and Treatment Options." INTERNATIONAL JOURNAL OF MEDICAL SCIENCE AND CLINICAL RESEARCH STUDIES ISSN 04, no. 04 (2024): 645–50. https://doi.org/10.5281/zenodo.10948940.

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Meckel's diverticulum (MD) is a common congenital anomaly of the gastrointestinal tract, characterized by an outpouching in the terminal ileum. It can be symptomatic in various ways, most commonly causing ulcers and gastrointestinal bleeding. Complications such as bleeding, perforation, diverticulitis, or intestinal obstruction may develop in approximately 4% of patients. Diagnosis can be challenging, but a CT scan is often the tool of choice, particularly for identifying complications. Surgical procedures like laparoscopy or laparotomy provide a more accurate diagnosis. Treatment typically in

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Pervez, Hira. "Triple Lumen Esophagus; A Rare Congenital Anomaly Presenting with Dysphagia." Research International Journal of Surgery and Medicine 01, no. 01 (2020): 004–6. http://dx.doi.org/10.37179/rijsm.000002.

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Alimentary tract duplications are rare congenital malformations that can occur at any level of the gastrointestinal (GI) tract from mouth to anus. Triple lumen esophagus is even rarer occurrence and has not been reported previously according to our literature search. The diagnosis is often confused with esophageal tract duplication secondary to perforation or surgeries leading to Gastroesophageal 􀏐istula formation. A middle-aged female presented to us with an intermittent history of dysphagia and gastroesophageal re􀏐lux disease (GERD) and was diagnosed with a triple lumen esophagus radiographi

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17

TARIQ, SAADIA. "CONGENITAL ANOMALIES IN NEWBORN." Professional Medical Journal 17, no. 01 (2010): 135–39. http://dx.doi.org/10.29309/tpmj/2010.17.01.2094.

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Objective: To determine congenital anomalies in newborn and associated maternal risk factors. Design: Cross sectionalobservational study. Setting: Department of Gynecology & Obstetrics unit 1 Lahore General Hospital Lahore. Period: From Jan 2007—Dec2007. Patients & methods: All the women who have given birth to babies with congenital abnormalities were recorded. Diagnosis of neonatalcongenital anomalies was based on clinical evaluation of newborn by experienced neonatologist. Results: During the study period, 2872patients delivered, of which 48 had congenitally malformed babies, makes

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18

Jindal, Deepti, Varun Jindal, Himanshu Singh, Swati Gautam, Ishita Bhojia, and Arjun Chaudhary. "Agenesis of Bilateral Permanent Mandibular Canine: A Rare Case Report." Dental Journal of Advance Studies 04, no. 01 (2016): 056–58. http://dx.doi.org/10.1055/s-0038-1672046.

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AbstractHypodontia is the congenital absence of less than six teeth because of agenesis. Congenital absence of tooth (hypodontia) from the dental arch, may occur with any tooth, most commonly being third molars, however, absence of permanent mandibular canine is rare. The absence of teeth may be unilateral or bilateral. There are reports showing unilateral occurrence of permanent mandibular canines but agenesis of bilateral mandibular canines is not well documented in the literature and comprehensive review of literature shows paucity of data pertaining to this anomaly. Here we report one such

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19

Ene, Claudia-Andreea, Georgiana Olaru-Lego, Ioan-Mircea Coman, Pavel Platon, and Adrian Mereuță. "Complex Congenital Heart Lesion - Should We Operate or Not?" Romanian Journal of Cardiology 34, no. 2 (2024): 86–91. http://dx.doi.org/10.2478/rjc-2024-0010.

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Abstract Congenitally corrected transposition of the great arteries (ccTGA) is a rare congenital anomaly defined by double discordance – atrioventricular and ventricular-arterial. ccTGA frequently has associated lesions, which influence long-term survival. The management of patients with ccTGA regarding the closure of defects and pacing strategies is often very challenging. Moreover, tricuspid valve regurgitation and its impact on the systemic right ventricle requires close monitoring and potentially timely interventions. In this paper, we present and discuss the management challenges raised b

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20

Khan, Shazia Amir, Iram Iqbal, Fouzia Rasheed, Khizra Anwar, Ammara Nadeem, and Menahyl Mahmood. "A Single Centre Retrospective Study to Access the Frequency of Congenital Anomalies in a Tertiary Care Hospital." Journal of HBS M&DC 3, no. 2 (2024): 48–50. http://dx.doi.org/10.70394/jhbsmdc.v3i2.50.

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Objectives: The objective of our study was to determine the frequency and types of congenital fetal anomalies among pregnant patient in tertiary care hospital. Methodology: This is descriptive, cross sectional retrospective study conducted in obstetrics and gynecology and radiology department of HBS General hospital Islamabad from January 2021 to January 2023.It includes all booked and unbooked antenatal patients Results: Over a period of two years total 3723 antenatal patients included in our study out of which 2.01% were diagnosed with congenitally structurally malformed fetuses. Commonly ob

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21

Dhanasekar, P. Durai, Sushanth N K, and Lakshmi kantha B M. "RETROSPECTIVE STUDY OF FETAL CONGENITAL ANOMALY IN WAYANAD TERTIARY CARE CENTRE." International Journal of Anatomy and Research 8, no. 3.1 (2020): 7599–603. http://dx.doi.org/10.16965/ijar.2020.171.

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22

Sahoo, Bismayee, and Santosh Kumar Behera. "A Case Series on Amniotic Band Syndrome Presenting as Congenital Anomaly." International Journal of Science and Research (IJSR) 14, no. 2 (2025): 679–81. https://doi.org/10.21275/sr25210213100.

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23

Ozturk, Selcuk, Fatma Erdem, Serkan Ozturk, and Selim Ayhan. "Successful thrombolytic therapy in a patient with congenital corrected transposition of the great arteries." Acta Medica Academica 45, no. 2 (2016): 150. http://dx.doi.org/10.5644/ama2006-124.172.

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<p><strong>Objective</strong>. The aim of this report is to emphasize the importance of thrombolytic therapy in selected patients, such as those with congenital heart defects in whom a coronary artery anomaly can be observed. <strong>Case report</strong>. We present here a 63 year-old female patient who was admitted to our emergency department with ST segment elevation myocardial infarction and a history of a congenital heart defect. We treated the patient successfully with thrombolytic therapy instead of primary percutaneous intervention, because of the suspicion

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Petrovna, Askaryans Vera, and Xikmatov Javoxirbek Sherali ogli. "CONGENITAL HEART DEFECTS." Eurasian Journal of Medical and Natural Sciences 03, no. 02 (2023): 194–99. http://dx.doi.org/10.37547/ejmns-v03-i02-p1-32.

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Congenital heart defects (TYN), also known as congenital heart anomaly and congenital heart disease, are defects in the structure of the heart or great vessels present at birth. Congenital heart defects are classified as cardiovascular diseases. Signs and symptoms depend on the specific type of defect. Symptoms can be harmless or life-threatening. If present, symptoms may include rapid breathing, bluish skin (cyanosis), low weight, and fatigue. Congenital heart defects do not cause chest pain. Congenital heart defects are often not associated with other diseases. A complication of congenital h

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Boo-Chai, Khoo, and Chae Cho Byun. "CONGENITAL ANOMALIE." Plastic and Reconstructive Surgery 91, no. 7 (1993): 1376. http://dx.doi.org/10.1097/00006534-199306000-00060.

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26

Couy, Matheus Pimenta, Gustavo Dall’Orto Giuriato, Larissa Soares Miranda Boaventura, and Thais Camila Alves Lessa Duran. "INCIDÊNCIA DE DEFORMIDADES CONGÊNITAS DO APARELHO OSTEOMUSCULAR EM RONDÔNIA ENTRE 2013 E 2021." REVISTA FIMCA 11, no. 1 (2024): 17–19. http://dx.doi.org/10.37157/fimca.v11i1.856.

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Introdução: As malformações congênitas são desenvolvidas durante o período intraútero e podem repercutir em alterações morfológicas e funcionais significantes. A mais comum entre elas é a anomalia congênita osteomuscular, que costuma acometer principalmente quadril e pés dos neonatos. Objetivo: Verificar a incidência de deformidades congênitas osteomusculares no estado de Rondônia, analisar qual a distribuição entre deformidades congênitas de quadril e de pé, e avaliar a qualidade dos pré-natais dos casos notificados. Materiais e Métodos: Pesquisa de caráter transversal, através do Sistema de

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27

Aguiar, Michelle Alves Viana, and Anelise Riedel Abrahão. "Post-traumatic stress disorder and congenital anomalies in prenatal care." Revista Brasileira de Saúde Materno Infantil 22, no. 3 (2022): 517–25. http://dx.doi.org/10.1590/1806-9304202200030005.

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Abstract Objective: to assess post-traumatic stress disorder (PTSD) symptoms in pregnant women diagnosed with congenital anomaly. Methods: his is a quantitative and cross-correlational study. The sample consisted of 111 pregnant women diagnosed with congenital anomaly between 2013 and 2014. We used a semi-structured questionnaire and the Impact of Events Scale - Revised (IES-R). For statistical analysis, the chi-square test, Student’s t test or Mann-Whitney test, Cronbach Alpha coefficients, Pearson’s correlation and simple linear regression models. Results: viable congenital anomalies corresp

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Galea, Joseph, Sarah Ellul, Aaron Schembri, Pierre Schembri-Wismayer, and Jean Calleja-Agius. "Ebstein Anomaly: A Review." Neonatal Network 33, no. 5 (2014): 268–74. http://dx.doi.org/10.1891/0730-0832.33.5.268.

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Cardiac congenital abnormalities are a leading cause in neonatal mortality occurring in up to 1 in 200 of live births. Ebstein anomaly, also known as Kassamali anomaly, accounts for 1 percent of all congenital cardiac anomalies. This congenital abnormality involves malformation of the tricuspid valve and of the right ventricle. In this review, the causes of the anomaly are outlined and the pathophysiology is discussed, with a focus on the symptoms, management, and treatments available to date.

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Rao, Suresh R., Ovchinnikov Nikolai, Jagessar Avinash, Ramesh T. Rao T, Somu S. Gajula, and Chalapathi A. V. Rao. "AN UNUSUAL CASE OF CONGENITAL ANOMALY OF THE HEART. Un caso poco común de anomalía congénita del corazón." Revista Argentina de Anatomía Clínica 3, no. 1 (2016): 57–63. http://dx.doi.org/10.31051/1852.8023.v3.n1.13916.

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La creciente utilización de diagnósticos invasivos y procedimientos de intervención en enfermedades cardiovasculares han enfatizado la importancia de entender y documentar mejor el tipo y la frecuencia de las variaciones vasculares. Los defectos del corazón se encuentran entre las anomalías congénitas más comunes. Estas pueden ser simples o complejas. En la mayoría de las anomalías congénitas del corazón se requiere intervención quirúrgica para garantizar la vida. Los médicos y cirujanos deben ser educados sobre las distintas formas de enfermedades congénitas del corazón para facilitarles su m

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30

Úraga, Enrique, Verónica Úraga, Karla Garcés, and Andrea Aguilar. "Trago Accesorio Asociado a Otras Alteraciones. Una Recopilación Visual de Casos Observados y Una Revisión Suscinta del Tema." Revista Dermatológica Centro Uraga 4, no. 1 (2022): 62–79. https://doi.org/10.63787/4.1.2022.62-79.

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El trago accesorio es una anomalía congénita del primer arco branquial de observación relativamente infrecuente. Si bien existen reportes de asociación con otras patologías, congénitas o no, estas si son muy escasas. Realizamos una revisión de dichas asociaciones y presentamos de manera muy suscinta algunos casos de nuestra consulta con el afán de mostrar la existencia de estas asociaciones en nuestro medio. Por tratarse de una exposición visual de estas asociaciones en su mayor parte congénitas, las historias clínicas no son expuestas. The accessory tragus is a relatively uncommon congenital

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Chubanovová, Nikoleta, Roman Chmel, Roland Kelčík, Jana Nováková, and Marta Nováčková. "Hymenal atresia – a rare congenital anomaly with the risk of late diagnosis." Česká gynekologie 87, no. 2 (2022): 118–23. http://dx.doi.org/10.48095/cccg2022118.

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Objective: Comprehensive analysis of causes, clinical signs, diagnostic process, differential diagnosis and therapy of hymenal atresia. Methods: Literature search using the Web of Science, Google Scholar and PubMed databases with keywords and analysis of articles published in high impact and reviewed journals. Results: Hymenal atresia is a congenital malformation of a woman's genitals, which is manifested by complete obstruction of the vaginal introitus by a closed hymen. It should be diagnosed in the neonatal period, but clinically it usually manifests itself only during puberty as a result o

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32

Tiwari, Pawan, Aman Yadav, Madhu Tiwari, et al. "Horseshoe Appendix: Report of Extremely Rare Congenital Anomaly with Review of Literature." International Journal of Science and Research (IJSR) 14, no. 1 (2025): 48–50. https://doi.org/10.21275/mr241218211821.

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S, K. Gupta, Singh Saurabh, Singh Kameshwar, and Maurya Vivek. "Macrodactyly- A case report." Advance Research Journal of Multidisciplinary Discoveries 75, no. 1 (2022): 05–07. https://doi.org/10.5281/zenodo.7066422.

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Macrodactyly is a rare non-hereditary congenital anomaly of finger and toes and it is very difficult to treat this, as it largely depends on exposure of surgeon to the disease process. The disease process may be static or progressive. It accounts for about 1% of upper extremity congenital anomalies. Usually involve fibrofatty tissue and sometimes bones. The first detail study was done by Barsky in 1967. It is linked with mutation in the PIK3CA gene which control cell proliferation and migration. Barsky defined it as an increase in size of all the elements or structures within a digit or digits

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Choi, So-Young, and Mila Lee. "Experience of Mothers who Gave Birth to Congenitally Anomalic Babies." Korean Journal of Women Health Nursing 3, no. 1 (1997): 22–30. http://dx.doi.org/10.4069/kjwhn.1997.3.1.22.

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Recently, the birth rate of congenitally anomalic babies is increasing in Korea. But there are few studies and articles in nursing field. So nurses are having difficulties in caring those mothers. This study is to reveal experiences of the mothers with congenitally anomalic babies. Subjects were six and data were gathered by interviews. Data were analyzed by Giorgi's method. Mother's responses were organized into five categories-shock, sadness, expectation, attribution and loss of confidence on future pregnancies. Loss of confidence on future pregnancies were categories which were not found in

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Bove, Edward L., Richard G. Ohye, Eric J. Devaney, et al. "Anatomic correction of congenitally corrected transposition and its close cousins." Cardiology in the Young 16, S3 (2006): 85–90. http://dx.doi.org/10.1017/s1047951106001132.

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The congenital cardiac malformation characterized by discordant connections between the atriums and ventricles, as well as those between the ventricles and the arterial trunks, has been given many names. The terms atrioventricular discordance, l-transposition of the great arteries, ventricular inversion, and congenitally corrected transposition have all been used. Regardless of terminology, this complex congenital anomaly has only recently been studied to analyze the long-term effects of its natural history and outcomes following traditional surgical repair of the associated malformations whic

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Bove, Edward L., Richard G. Ohye, Eric J. Devaney, et al. "Anatomic correction of congenitally corrected transposition and its close cousins." Cardiology in the Young 16, S3 (2006): 85–90. http://dx.doi.org/10.1017/s1047951106001399.

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The congenital cardiac malformation characterized by discordant connections between the atriums and ventricles, as well as those between the ventricles and the arterial trunks, has been given many names. The terms atrioventricular discordance, l-transposition of the great arteries, ventricular inversion, and congenitally corrected transposition have all been used. Regardless of terminology, this complex congenital anomaly has only recently been studied to analyze the long-term effects of its natural history and outcomes following traditional surgical repair of the associated malformations whic

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Park, Hun Yi, Dong Hee Han, Jong Bin Lee, Seong Jun Choi, Yun-Hoon Choung, and Keehyun Park. "Isolated Congenital Incus Anomaly." Korean Journal of Otolaryngology-Head and Neck Surgery 52, no. 4 (2009): 335. http://dx.doi.org/10.3342/kjorl-hns.2009.52.4.335.

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38

Czeizel, Andrew, John M. Optiz, and James F. Reynolds. "Additive congenital anomaly patterns." American Journal of Medical Genetics 29, no. 4 (1988): 727–38. http://dx.doi.org/10.1002/ajmg.1320290402.

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Bagus, Setyoboedi, Aji Prihaningtyas Rendi, and Arief Sjamsul. "Caroli's Disease in a Child: A Rare Case Report." INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND BIO-MEDICAL SCIENCE 04, no. 07 (2024): 603–7. https://doi.org/10.5281/zenodo.12670153.

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<strong>Introduction:</strong> Caroli's disease is a rare hereditary condition. It is characterized by segmental dilatation of the large intrahepatic bile duct with a cyst-like appearance. Caroli's disease is often found on typical imaging without specific symptoms. It can lead to progressive bile duct obstruction and cirrhosis. Therefore, early diagnosis and appropriate treatment are necessary for optimal outcomes and prognosis.   <strong>Case presentation:</strong> A 12-month-old girl presented to the outpatient clinic of Dr. Soetomo General Academic Hospital, Surabaya, with c

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Roul, Pradeep Kumar, Aditi Saini, Srishti Agarwal, Prashant Kumar Verma, and Anjum Syed. "Bilobed gallbladder: a rare congenital anomaly of the biliary system." International Journal of Research in Medical Sciences 9, no. 12 (2021): 3729. http://dx.doi.org/10.18203/2320-6012.ijrms20214730.

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Duplication of the gallbladder is a rare congenital anomaly, which Boyden first illustrated in 1926. No additional risk of cholelithiasis or malignancy with this congenital anomaly was documented. However, this congenital anomaly is associated with more risk for complications during and after laparoscopic cholecystectomy. So, preoperative diagnosis is essential in identifying anatomical abnormalities to avoid biliary injuries at the time of surgery or the performance of an incomplete operation. The removal of an asymptomatic double gallbladder remains controversial. Here, we are reporting a ca

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Boyle, Breidge, Marie-Claude Addor, Larraitz Arriola, et al. "Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data." Archives of Disease in Childhood - Fetal and Neonatal Edition 103, no. 1 (2017): F22—F28. http://dx.doi.org/10.1136/archdischild-2016-311845.

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ObjectiveTo validate the estimates of Global Burden of Disease (GBD) due to congenital anomaly for Europe by comparing infant mortality data collected by EUROCAT registries with the WHO Mortality Database, and by assessing the significance of stillbirths and terminations of pregnancy for fetal anomaly (TOPFA) in the interpretation of infant mortality statistics.Design, setting and outcome measuresEUROCAT is a network of congenital anomaly registries collecting data on live births, fetal deaths from 20 weeks’ gestation and TOPFA. Data from 29 registries in 19 countries were analysed for 2005–20

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Calzolari, F., G. Mescoli, G. Garani, V. Mazzeo, L. Tamisari, and P. Guerrini. "Anomalie congenite del bulbo oculare e del nervo ottico." Rivista di Neuroradiologia 9, no. 6 (1996): 663–68. http://dx.doi.org/10.1177/197140099600900606.

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Sono descritti sei casi di anomalie congenite del bulbo oculare e del nervo ottico. Diverse cause, genetiche o acquisite, possono alterare il normale sviluppo dell'organo della vista; il tipo di anomalia dipende dal momento in cui si verifica l'insulto o l'arresto di sviluppo piuttosto che dal fattore eziologico specifico. Il microftalmo viene definito «semplice» quando l'occhio è di piccole dimensioni ma normoconformato, «complesso» quando l'occhio è malformato. Il microftalmo complesso puù essere ulteriormente diviso in due categorie: forma colobomatosa e non colobomatosa; il coloboma è una

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Katargina, L. A., A. V. Pleskova, and A. V. Khvatova. "CONGENITAL CORNEAL OPACITIES." Russian Pediatric Ophthalmology 5, no. 2 (2010): 46–50. https://doi.org/10.17816/rpoj37472.

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The article is dedicated to the clinical picture and diagnostics as well as the principles of management of pediatric patients with corneal opacity of various genesis including congenital malformations of the anterior section of the eye (posterior embryotoxon, Axenfeld anomaly, Rieger anomaly, Peters anomaly, corneal staphyloma, sclerocornea). Clinical picture of the congenital dystrophy and benign tumors of the cornea and limbus as well as the corneal opacities in congenital glaucoma, metabolic lesions and intrauterine infection is presented.

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Wang, Hao, Ewa Wender-Ozegowska, Ester Garne, et al. "Insulin analogues use in pregnancy among women with pregestational diabetes mellitus and risk of congenital anomaly: a retrospective population-based cohort study." BMJ Open 8, no. 2 (2018): e014972. http://dx.doi.org/10.1136/bmjopen-2016-014972.

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ObjectivesTo evaluate the risk of major congenital anomaly associated with first-trimester exposure to insulin analogues compared with human insulin in offspring of women with pregestational diabetes.Design and settingA population-based cohort of women with pregestational diabetes (n=1661) who delivered between 1996 and 2012 was established retrospectively from seven European regions covered bythe European Surveillance of Congenital Anomalies (EUROCAT) congenital anomaly registries.Primary outcome measuresThe risk of non-chromosomal major congenital anomaly in live births, fetal deaths and ter

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Piovesana, Piergiuseppe. "Valutazione delle arterie coronariche con ecocardiografia transtoracica." Cardiologia Ambulatoriale 1, no. 32 (2024): 61–73. http://dx.doi.org/10.17473/1971-6818-2024-1-7.

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In questo articolo vengono descritte le varie metodiche ecocardiografiche che consentono di diagnosticare con buona accuratezza le anomalie congenite delle aa. Coronariche (AOAC) individuando i soggetti a rischio che verranno poi indirizzati verso altre tecniche di imaging, in particolare la TC coronarica, per una ottimale definizione dell’anomalia anatomica. Le AOAC rappresentano una malformazione congenita abbastanza rara. Generalmente i difetti congeniti di origine delle aa. Coronariche dal Seno di Valsalva opposto hanno una prognosi favorevole, tuttavia esistono alcune forme che per la par

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Amani, Fariska Zata, Wardhana M. P, Cininta N. I, et al. "Clinical Characteristic of Congenital Fetal Anomaly In Tertiary Referral Hospital in East Java, Indonesia." International Islamic Medical Journal 2, no. 2 (2021): 40–46. http://dx.doi.org/10.33086/iimj.v2i2.1624.

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Background: Congenital fetal anomalies were defined as any structural defect present at birth. Congenital fetal anomalies are an important causes of neonatal morbidity and mortality in developed and developing countries that affect health care system. Reliable data on these congenital anomalies are still lacking, especially in Indonesia. Objective: This study aims to determine the characteristic profile of congenital fetal anomaly in single tertiary hospital in East Java, Indonesia. Methods: Retrospective cross-sectional by using medical record data of dr. Soetomo General Hospital on January –

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Talarico, M., M. Colangelo, F. Cassadonte, and V. Ciconte. "P179 RISCONTRO ACCIDENTALE DI UN RARO CASO DI COR TRIATRIUM DESTRO ASSOCIATO A DIFETTO INTER–ATRIALE IN UN PAZIENTE ADULTO." European Heart Journal Supplements 25, Supplement_D (2023): D109—D110. http://dx.doi.org/10.1093/eurheartjsupp/suad111.258.

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Abstract Background Il cor triatrium destro (CTD), anomalia congenita in cui l’atrio sinistro è settato da una membrana in due parti, è un rilievo estremamente raro: in centri ad alti volumi la prevalenza è inferiore allo 0.01% (1). Il cor triatriatum destro è spesso associato ad alter anomalie congenite quali anomalie della valvola polmonare, il ventricolo destro ipoplasico, l’anomalia di Ebstein, i difetti del setto inter–atriale (DIA) (2,3). Quando la settazione è incompleta può essere asintomatico e riscontrato accidentalmente all’esame ecocardiografico (4). Descrizione del caso: A dicembr

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Marler, Adam T., Jennifer N. Slim, Travis Batts, James Watts, and Ahmad M. Slim. "A Case of Congenitally Corrected Transposition of the Great Arteries Discovered on Coronary Computed Tomography." Case Reports in Vascular Medicine 2013 (2013): 1–3. http://dx.doi.org/10.1155/2013/420213.

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Congenitally corrected transposition of the great arteries is a rare condition accounting for less than 1% of all congenital cardiac diseases. The fundamental nature of this condition involves a blend of atrioventricular as well as ventriculoarterial discordance. Congenitally corrected transposition of the great arteries is classically associated with three additional abnormalities, including ventricular septal defect, right ventricular outflow tract obstruction, and tricuspid valve abnormalities. Patients with this anomaly have been shown to exhibit reduced exercise tolerance as well as reduc

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Sinelnikov, Yu S., R. M. Shekhmametyev, A. S. Vronsky, and P. V. Lazarkov. "Surgical treatment of vascular ring resulting in the formation of left aortic arch." Complex Issues of Cardiovascular Diseases 11, no. 1 (2022): 135–39. http://dx.doi.org/10.17802/2306-1278-2022-11-135-139.

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Highlights. The described clinical case of surgical treatment of congenital anomaly of the aortic arch is of high interest to specialists due to the relatively late manifestation of symptoms, low incidence of the anomaly, prior surgical treatment of congenital heart disease in medical history, and characteristics of surgical intervention.Background. The described clinical case reports successful treatment of vascular ring formed by right aortic arch with aberrant left subclavian artery. The described clinical case of surgical treatment of congenital anomaly of the aortic arch is of high intere

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Rao, P. Syamasundar. "Echocardiography: an overview - Part III." Vessel Plus 6 (2022): 26. http://dx.doi.org/10.20517/2574-1209.2021.93.

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This review describes echocardiographic features of commonly encountered cyanotic congenital heart defects. Echo-Doppler characteristics of more commonly seen defects: tetralogy of Fallot, transposition of the great arteries, tricuspid atresia, total anomalous pulmonary venous connection, and truncus arteriosus were first discussed. Then, hypoplastic left heart syndrome followed by less commonly observed lesions such as double-outlet right ventricle, double-inlet left ventricle, interrupted aortic arch, pulmonary atresia with an intact ventricular septum, congenitally corrected transposition o

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