Relevant bibliographies by topics / Congenital anomally

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Congenital anomally'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Congenital anomally"

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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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Congenital anomally"

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Halpin, Lisa. "Foetal congenital anomaly diagnoses and maternal mental health." Thesis, University of Liverpool, 2017. http://livrepository.liverpool.ac.uk/3009541/.

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Pregnancy is a time of physiological and psychosocial change for women, and can be a stressful life event (Hodgkinson, Smith & Wittkowski, 2014). Therefore, for some women, pregnancy can exacerbate existing psychological distress (e.g. depression, anxiety and/or stress), or contribute to its development (Biaggi, Conroy, Pawlby & Pariante, 2016). Although there are many reasons why some women experience psychological distress during pregnancy (e.g. lack of social support; Biaggi et al., 2016), this thesis is concerned with the impact of foetal congenital anomaly diagnosis on maternal mental hea
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FORCIOLI, JEAN-MARIE. "Anomalie congenitale de l'artere vertebrale." Aix-Marseille 2, 1988. http://www.theses.fr/1988AIX20106.

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Taub, Nicholas Aaron. "Methods to assess ascertainment in congenital anomaly registers, with application to congenital heart defects." Thesis, University of Leicester, 2005. http://hdl.handle.net/2381/30485.

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Luteijn, Johannes Michiel. "2009 H1N1 pandemic influenza in Europe: congenital anomaly surveillance response." Thesis, University of Ulster, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.593634.

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Summary Introduction: This thesis reports the surveillance response of the EUROCAT network of population based registries for surveillance of congenital anomalies to the 2009 H1Nl influenza pandemic. Due to the controversy around vaccinating 1st trimester pregnant women, the relationship between pandemic influenza outbreaks and congenital anomalies (CA) deserves attention. The purpose of this thesis is to improve public health practice by investigating the effect of the 2009 HiNl influenza pandemic on CA prevalence in Europe and exploring the pandemic vaccination policy and policy making with
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Stryzhakovs’ka, L. O. "Congenital anomaly of the urinary tracts in 5-month old fetuses." Thesis, Буковинський державний медичний університет, 2012. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/1440.

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Busby, Aracelie Lorraine. "The epidemiology of anophthalmos / microphthalmos in England." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289756.

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Vrijheid, Martine. "Risk of congenital anomaly in relation to residence near hazardous waste landfill sites." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2000. http://researchonline.lshtm.ac.uk/682274/.

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The main aim of this thesis is to investigate whether residence near hazardous waste landfill sites is associated with an increased risk of congenital anomaly. The thesis reports results of a multi-centre case-control study carried out in 10 regions in 6 European countries. Cases were live births, stillbirths, and induced abortions with major congenital anomalies resident at birth within a 7 km area around hazardous waste landfill sites. Controls, two per case, were non-malformed births resident in the same area. A total of 1089 cases of non-chromosomal anomaly, 270 cases of chromosomal anomal
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Colarusso, Tiffany. "Descriptive Analysis of Ebstein Anomaly in the National Birth Defects Prevention Study, 1997-2007." Digital Archive @ GSU, 2012. http://digitalarchive.gsu.edu/iph_theses/210.

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There is relatively little epidemiologic information about Ebstein anomaly (EA) ─ a rare congenital heart defect. Thus, we analyzed characteristics of EA in a geographically and ethnically diverse population. Data from the National Birth Defects Prevention Study were used to study infants born from 1997-2007 with EA. Birth prevalence and prevalence ratio (PR) estimates were derived from the number of affected infants per 10,000 live births in the catchment area. Case characteristics were examined, stratified by the presence of other cardiac and extracardiac defects. Predictive modeling usi
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Goldsmith, Shona. "Population studies of assisted reproductive technology and congenital anomalies in cerebral palsy." Thesis, The University of Sydney, 2019. https://hdl.handle.net/2123/21909.

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BACKGROUND: Risk factors for cerebral palsy (CP) have been identified across the conception, pregnancy, perinatal and postneonatal periods, including Assisted Reproductive Technology (ART) and congenital anomalies. ART likely increases risk of CP through mediating factors including multiple and preterm birth, but this requires further investigation in Australia. While congenital anomalies are an identified risk factor for CP, their reported prevalence varies widely. This thesis describes the epidemiology of CP with respect to these two independent factors. METHODS: A series of population-based
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Machu, Isabelle. "Anomalies congenitales des voies biliaires chez l'enfant : a propos de dix observations." Lille 2, 1994. http://www.theses.fr/1994LIL2M150.

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Books on the topic "Congenital anomally"

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Great Britain. Office for National Statistics., ed. Congenital anomaly statistics: Notifications : a statistical review of notifications of congenital malformations receivedas part of the England and Wales national congenital anomaly system. Stationery Office., 1997.

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Great Britain. Office for National Statistics. Congenital anomaly statistics: Notifications: a statistical review of notifications of congenital anomalies received as part of the England and Wales Congenital Anomaly System, 2001. Stationery Office, 2002.

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Hras̆ka, Viktor. Surgical management of congenital heart disease I: Complex transposition of great arteries right and left, ventricular outflow, tract obstruction, Ebsteins anomaly : a video manual. Springer, 2012.

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British Isles Network of Congenital Anomaly Registers. Congenital Anomaly Statistics 2010. Dandy Booksellers Ltd, 2013.

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Statistics, Office for National. Congenital Anomaly Statistics Notification. Palgrave Macmillan, 2006.

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Statistics, Office for National. Congenital Anomaly Statistics (Series MB3). Stationery Office Books, 1998.

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Statistics, Office for National. Congenital Anomaly Statistics (Series MB3). Stationery Office Books, 1999.

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The Office for National Statistics. Congenital Anomaly Statistics Notification 2007 No. 22. Palgrave Macmillan Limited, 2009.

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NA, NA. Congenital Anomaly Statistics Notification 2003 No. 18. Palgrave Macmillan, 2005.

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NA, NA. Congenital Anomaly Statistics Notification 2005 No. 20. Palgrave Macmillan, 2007.

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Book chapters on the topic "Congenital anomally"

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Corno, Antonio F. "Ebstein’s anomaly." In Congenital Heart Defects. Steinkopff, 2003. http://dx.doi.org/10.1007/978-3-642-57358-3_11.

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Connolly, Heidi M. "Ebstein's Anomaly." In Adult Congenital Heart Disease. Blackwell Publishing Ltd., 2009. http://dx.doi.org/10.1002/9781444311846.ch12.

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Corno, Antonio F. "Erratum to: Ebstein’s anomaly." In Congenital Heart Defects. Steinkopff, 2003. http://dx.doi.org/10.1007/978-3-642-57358-3_20.

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Kives, Sari. "Müllerian Anomaly Classification Systems." In Congenital Müllerian Anomalies. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-27231-3_1.

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Girnius, Andrea, Gruschen Veldtman, Carri R. Warshak, and Markus Schwerzmann. "Ebstein Anomaly." In Pregnancy and Congenital Heart Disease. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-38913-4_14.

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Dearani, Joseph A., and Constantine Mavroudis. "Ebstein Anomaly." In Atlas of Adult Congenital Heart Surgery. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-14163-9_17.

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Sridharan, Shankar, Gemma Price, Oliver Tann, Marina Hughes, Vivek Muthurangu, and Andrew M. Taylor. "Ebstein's Anomaly." In Cardiovascular MRI in Congenital Heart Disease. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-69837-1_52.

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Shah, Pratibha Jain. "Craniosynostosis: A Congenital Anomaly." In Clinical Anesthesia for the Newborn and the Neonate. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-19-5458-0_43.

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Park, In Sook, Soo-Jin Kim, and Hyun Woo Goo. "Ebstein’s Anomaly." In An Illustrated Guide to Congenital Heart Disease. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6978-0_17.

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Barthur, Ashita, and Salil Bhargava. "Ebstein Anomaly." In CT and MRI in Congenital Heart Diseases. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-6755-1_13.

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Conference papers on the topic "Congenital anomally"

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Zia, Muhammad, Mugahid Ibrahim, Iqtadar Hussain, and Cornelius Sreenan. "P648 Anonychia congenita: a rare congenital anomaly." In Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.979.

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Noman, Muhammad. "Congenital L-Transposition of the Great Arteries in a 12-Year-Old: A Case Report." In 27th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2023. https://doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.101_2023.

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Levo-transposition of the great arteries, L-TGA, also known as congenitally corrected transposition, cc-TGA is a rare anomaly and accounts for less than 1% of all congenital heart diseases. It is characterized by both atrioventricular and ventriculoarterial discordance . It is considered a congenitally corrected transposition because the circulation is from right atrium to left ventricle leading to the pulmonary vasculature. The lungs then pump blood into the left atrium to the right ventricle and eventually to the systemic circulation via the aorta.
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Hari Gopal, S., M. Kreth, and J. Ledbetter. "Congenital Bronchopulmonary Foregut Malformation with VACTERL Anomaly." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a5367.

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Davidst, Adeniji Oluwashola, Omopintemi Ayorinde Henry, and Samuel Oladele Adeyemi. "Prediction of Congenital Anomaly Using Deep Learning Techniques." In 2023 First International Conference on the Advancements of Artificial Intelligence in African Context (AAIAC). IEEE, 2023. http://dx.doi.org/10.1109/aaiac60008.2023.10465280.

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Ciriaco, Debora, Alexandre Pessoa, Lais Salvador, and Renata Wassermann. "Semantic Data Integration for Public Health in Brazil." In LatinX in AI at International Conference on Machine Learning 2019. Journal of LatinX in AI Research, 2019. http://dx.doi.org/10.52591/lxai2019061514.

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The lack of semantic information is a big challenge, even in context-driven areas like Healthcare, characterized by established terminologies. Here, semantic data integration is the solution to provide precise information and answers to questions like: What is the care pathway of newborns diagnosed with a congenital anomaly in consequence of congenital syphilis in the city of Sao Paulo? This project will use a semantic data integration technique, ontology based data integration, to integrate three health databases from the city of Sao Paulo - Brazil: mortality, live births and hospital informa
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Eldhose, Ansha, S. Saravanamuthu, and N. Dhinakaran. "Bilateral Congenital Absence of Stapes Superstructure, Rare Ossicular Anomaly Managed Endoscopically." In 27th Annual National Conference of the Indian Society of Otology. Thieme Medical and Scientific Publishers Private Ltd., 2019. http://dx.doi.org/10.1055/s-0039-1700219.

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Tenhoff, Amanda C., Tinen L. Iles, Paul A. Iaizzo, and Robroy MacIver. "Aberrant Coronary Artery: A Rare Congenital Anomaly Examined Through Pre- And Post-Procedural 3D Anatomical Modeling." In 2022 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/dmd2022-1061.

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Abstract Congenital heart disease – structural abnormalities of the heart that are present at and persistent beyond birth – affects about one in every 100 live births every year in the United States [1]. One such disease is that of the aberrant coronary artery, which describes abnormalities of coronary artery morphology. In our case, we examine a patient exhibiting complex aberrant right coronary artery – a rare congenital heart defect. Pre- and post-procedural imaging was acquired from this case, and subsequent three-dimensional (3D) anatomical models were created. These models were used post
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Braganza, Melanie L., Fahad Saeed, and Sujay Bangarulingam. "Congenital Anomaly Of The Respiratory Tract Surfaces As Recurrent Pneumonias In An Adult." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a6177.

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Wang, Rui, Francois G. Lacour-Gayet, Craig Lanning, Kendall Hunter, and Robin Shandas. "Patient-Specific Fluid Structure Interaction Simulation Applied to Evaluating Hemodynamics Within the Total Cavopulmonary Connection." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176494.

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Congenital heart disease (CHD), a life-threatening birth disorder, is the most common genetic disorder with an incidence rate as high as 1% in neonates (36,000 cases in 2006). Amongst these children, one out of four has single ventricle anomaly. As a palliative rather than a curative means for vascular reconstruction, the “Fontan” palliation has been used to produce stable hemodynamic states, at least for a limited period of time. However, the majority of post-Fontan patients faces a high risk of mortality and morbidity [1], and will have to undergo heart transplant eventually due to the exces
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Govindarajan, V., H. S. Udaykumar, S. Vigmostad, et al. "Fluid Structural Interaction of a Patient Specific Congenital Bicuspid Aortic Valve." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80196.

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Congenital Bicuspid Aortic Valve (BAV) is a valvular anomaly where a patient is born with a valve with two leaflets instead of a normal tri-leaflet valve. It has also been reported that BAVs are prone to progressive calcification and also other complications such as ascending aortic dilatation, dissection and rupture [1]. The geometrical variations with the BAV may be a factor in altering the deformation and stresses on the leaflets resulting in calcification of the leaflets earlier than with normal tri-leaflet aortic valves. Altered flow patterns past BAV into the ascending aorta can also be
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