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Relevant bibliographies by topics / Congenital deformity

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Academic literature on the topic 'Congenital deformity'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Congenital deformity"

1

S Basu, Partha, Hazem Elsebaie, and MHH Noordeen. "Congenital Spinal Deformity." Spine 27, no. 20 (2002): 2255–59. http://dx.doi.org/10.1097/00007632-200210150-00014.

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Hall, Jonathan D., and Thomas R. Stevenson. "Congenital Ear Deformity." Annals of Plastic Surgery 21, no. 2 (1988): 145–48. http://dx.doi.org/10.1097/00000637-198808000-00010.

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Hart, Erin S., Brian E. Grottkau, and Jon C. Marino. "Congenital Coxa Vara Deformity." Orthopaedic Nursing 26, no. 6 (2007): 349–51. http://dx.doi.org/10.1097/01.nor.0000300944.01956.b8.

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Choudry, Q., R. Kumar, and P. G. Turner. "Congenital cleft foot deformity." Foot and Ankle Surgery 16, no. 4 (2010): e85-e87. http://dx.doi.org/10.1016/j.fas.2009.07.003.

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Yang, Cheng, Yuhui Chen, Zhen Li, et al. "Chondrocyte-Specific Knockout of TSC-1 Leads to Congenital Spinal Deformity in Mice." BioMed Research International 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/8215805.

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Congenital spinal deformity is the most severe clinical orthopedic issue worldwide. Among all the pathological processes of congenital spinal deformity, the imbalance of endochondral ossification is considered to be the most important developmental cause of spinal dysplasia. We established chondrocyte-specific TSC-1 knockout (KO) mice to overactivate the energy metabolic component, mammalian target of rapamycin complex 1 (mTORC1), and measured the spinal development by general, imaging, histological, and Western-blot assessments. In addition to skeletal dysplasia, the KO mice displayed severe

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MENNEN, U., and E. WILLIAMS. "Arthrogryposis Multiplex Congenita in a Monozygotic Twin." Journal of Hand Surgery 21, no. 5 (1996): 647–48. http://dx.doi.org/10.1016/s0266-7681(96)80150-1.

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Arthrogryposis multiplex congenita is a specific, well-defined congenital deformity which primarily affects muscles of limbs resulting in secondary joint deformities. The aetiology is still uncertain. One of monozygotic twin brothers with classical arthrogryposis multiplex congenita is presented, proving that this specific condition is not genetically transmitted.

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Chechelnitsky, D. I. "A case of congenital deformity." Kazan medical journal 32, no. 7 (2021): 616–17. http://dx.doi.org/10.17816/kazmj80656.

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Abraham, Edward, Bryan Waxman, Swati Shirali, and Michael Durkin. "Congenital Cleft-Foot Deformity Treatment." Journal of Pediatric Orthopaedics 19, no. 3 (1999): 404–10. http://dx.doi.org/10.1097/01241398-199905000-00023.

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Shaikh, Humza S., and Michael J. O'Malley. "Arthroplasty for Congenital Hip Deformity." Operative Techniques in Orthopaedics 29, no. 3 (2019): 100724. http://dx.doi.org/10.1016/j.oto.2019.100724.

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T, Sreenivas. "Congenital Distal Tibiofibular Synostosis - A Case Report." International Journal of Health Sciences and Research 11, no. 9 (2021): 178–80. http://dx.doi.org/10.52403/ijhsr.20210927.

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Congenital tibiofibular synostosis is the fusion of tibia and fibula since birth. So far there are many reports of congenital proximal tibio fibular synostosis in English literature, but congenital distal tibio fibular synostosis is very rarely described. Imaging studies by means of X rays, CT and MRI are required to rule out osteochondromas arising from distal tibia, fibula and other conditions. If the patient is symptomatic by means of deformity surgical intervention in the form of corrective osteotomy may be considered to prevent alternation of joint biomechanics. We report a rare case of c

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Dissertations / Theses on the topic "Congenital deformity"

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Wallander, Henrik M. "Congenital clubfoot aspects on epidemiology, residual deformity and patient reported outcome /." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-106366.

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Herman, Kazibwe. "Barriers experienced by parents/caregivers of children with clubfoot deformity attending specific clinics in Uganda." Thesis, University of the Western Cape, 2006. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_9901_1194348551.

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<p>Clubfoot is the most common congenital structural deformity that leads to physical impairments in children in many poor developing countries. Inadequately treated or neglected clubfoot has been found to be a common cause of ohysical disability globally among children and young growing adults. Many children are referred to the clinics for treatment but some parents do not comply with the treatment regimen whcih requires attending for consecutive treatment sessions. The purpose of this study was to investigate barriers to treatment attendance parents/caregivers of children with clubfoot encou

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Fernihough, Melissa. "Congenital facial deformity : experiences of mothers of twins." Diss., 2011. http://hdl.handle.net/10500/4935.

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The topic of cleft lip and/or palate is widely researched in literature. However no research to date has focused on mothers' experiences raising twins when one twin is born with a cleft lip and/or palate. This qualitative study aims to explore the unigue experiences of these mothers. The epistemological foundations of this study are postmodern, social constructionist and systemic. In accordance with a gualitative methodology data was collected in the form of the participants' personal written stories. This was done from a post-modern paradigm, from a systemic perspective. Themes that were extr

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Uccello, Valeria. "CONGENITAL FLEXURAL DEFORMITY IN THE FOAL: CASE SERIES." Tesi di dottorato, 2013. http://www.fedoa.unina.it/9566/1/UCCELLO_VALERIA_25.pdf.

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Flexural Deformities (FD) or “contractures” are a common disease in foals. Therapy to correct the defects is normally established in absence of a precise diagnosis and etiopathogenesis is usually unknown. In infants with weakness and/or contractures, a complete diagnostic algorithm is performed to identify the etiology and, afterwards, to begin the most appropriate therapy and a neuromuscular etiology has been supposed. Aims of the study were to describe a case series of congenital FD, to examine the role of the congenital neuromuscular diseases in etiology and pathogenesis of FD, to suggest a

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KOŠNÁŘOVÁ, Kateřina. "Problematika péče o dítě s pes equinovarus congenitus." Master's thesis, 2018. http://www.nusl.cz/ntk/nusl-391108.

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The area of the care of a Clubfoot (pes equinovarus congenitus PEC Clubfoot) Diagnosed Child is the topic of this Paper. Currently, the PEC is the second most frequent congenital deformity within orthopaedics. The theoretical part of this Paper deals with a description of the PEC, its diagnostics, cure and a possible risk of relapse. A sub-chapter of the Paper introduces the Achilleus association, which is the only body in the Czech Republic bringing together parents of PEC diagnosed children. The Paper also focuses on nurses and their role(s) in the nursing care of PEC diagnosed children.

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Popková, Zuzana. "Efektivita edukace dětských pacientů s vrozenou deformitou hrudní stěny ve FN Motol." Master's thesis, 2014. http://www.nusl.cz/ntk/nusl-337084.

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The aim of this paper was, at first, to evaluate the effectiveness of education of child patients with inborn deformation of pectoral wall in the University Hospital Motol in the MIRPE (Minimally Invasive Pectus Excavatum) operation correcting the inborn deformation of pectoral wall by using of a metal bar and for its surgery extraction after three years. At second, to map the effectiveness of education of child patients done by the hospital personnel during their hospitalization in the University Hospital Motol. This paper also presents its own opinions of both groups of respondents on the cu

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Rounová, Petra. "Vliv velikosti defektu a operační techniky na dlouhodobou morbiditu dětí s vrozenou brániční kýlou." Doctoral thesis, 2013. http://www.nusl.cz/ntk/nusl-328210.

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52 8 Summary The influence of defect size and surgical technique on the long-term morbidity of children with congenital diaphragmatic hernia Objective: The aim of this study is to evaluate the effects of diaphragm reconstruction using a synthetic non-absorbable patch from polytetrafluoroethylene (PTFE, Gore-Tex) and primary repair of diaphragm defects on the long-term morbidity in children after surgery of congenital diaphragmatic hernia (CDH), with a primary interest in the influence of these techniques on the occurrence of skeletal deformities and the development of pulmonary functions. One

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Books on the topic "Congenital deformity"

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Fairbank, Jeremy. Congenital scoliosis and kyphosis. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.003011.

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Levine, Laurence A., William Brant, and Stephen M. Larsen. Peyronie’s disease, congenital curvature, and chordee. Edited by David John Ralph. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0108.

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Penile curvature is usually secondary to Peyronie’s disease, which is a fibrotic wound healing disorder of the tunica albuginea. Other causes include congenital penile curvature and chordee. Penile deformity, if severe, results in significant difficulties with sexual intercourse and may make sexual intercourse impossible. The mainstay of treatment, if the deformity is stable and interfering with intercourse is surgery, while a variety of surgical treatments exist. Side effects of treatment include penile shortening, erectile dysfunction, and recurrent deformity. Medical treatments are usually

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Uglow, Michael. Congenital talipes equinovarus. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.013021.

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♦ Aetiology of idiopathic congenital talipes equinovarus remains unknown♦ Antenatal diagnosis is common with good differentiation of the idiopathic from the syndromic foot♦ The Ponseti method is the treatment of choice: results are poorer in the atypical and syndromic feet♦ Surgery is required in selected cases as the primary treatment and in others, as treatment for residual and/or recurrent deformity.

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Kainth, Daraspreet Singh, Karanpal Singh Dhaliwal, and David W. Polly. Spinal Deformity and Scoliosis. Edited by Mehul J. Desai. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199350940.003.0021.

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Spinal deformity can be present in children, adolescents, and adults. Early-onset scoliosis, which affects children less than 10 years of age, can be the result of congenital abnormalities or neuromuscular disease or can be idiopathic. Adolescents most commonly develop scoliosis as the result of adolescent idiopathic scoliosis. Adult deformity can be the result of progression of conditions present in childhood or adolescence, or from degenerative changes. Many conditions can lead to spine deformity, including congenital causes, trauma, cancer, osteoporosis, postsurgical, and idiopathic causes.

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G. H. (George Hart) 1883-1959 Hart. Acorn Calves: A Nonhereditary Congenital Deformity Due to Maternal Nutritional Deficiency; B699. Creative Media Partners, LLC, 2021.

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G. H. (George Hart) 1883-1959 Hart. Acorn Calves: A Nonhereditary Congenital Deformity Due to Maternal Nutritional Deficiency; B699. Creative Media Partners, LLC, 2021.

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Beyond the Grip of Craniosynostosis: An Inside View of Life Touched by the Congenital Skull Deformity. McFarland & Company, Incorporated Publishers, 2015.

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Johnstun, Kase D. Beyond the Grip of Craniosynostosis: An Inside View of Life Touched by the Congenital Skull Deformity. McFarland & Company, Incorporated Publishers, 2015.

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The spectacle of deformity: Freak shows and modern British culture. University of California Press, 2010.

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Dalal, Priti G., and Meghan Whitley. Pectus Excavatum. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0018.

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Pectus excavatum is a funnel-shaped congenital deformity of the chest. Although the deformity can appear minimal at birth, it may be progressive. There may be cardiac or pulmonary compromise in addition to subjective complaints of pain and shortness of breath. Management ranges from breathing exercises to surgical repair with mobilization of the sternum and ribs. This can be performed using an open or thoracoscopic technique. Complications of surgical repair include atelectasis and pneumothorax. Significant pain is associated with the surgical procedures and multimodal analgesic therapy, inclu

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Book chapters on the topic "Congenital deformity"

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Kosztowski, Thomas, Rafael De la Garza Ramos, C. Rory Goodwin, and Daniel M. Sciubba. "Congenital Thoracolumbar Deformity Complication." In Spinal Deformity. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60083-3_15.

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Demirci, Nuri, Caglar Yilgor, and Ahmet Alanay. "Congenital Spinal Deformity." In Orthopaedics and Trauma. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-30518-4_84.

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Rayan, Ghazi M., and Joseph Upton III. "Madelung Deformity." In Congenital Hand Anomalies and Associated Syndromes. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-54610-5_14.

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Manske, M. Claire, Michelle A. James, and H. Relton McCarroll. "Madelung’s Deformity." In Congenital Anomalies of the Upper Extremity. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-64159-7_25.

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Sibbel, Sarah E., Andrea S. Bauer, and H. Relton McCarroll. "Madelung Deformity." In Congenital Anomalies of the Upper Extremity. Springer US, 2014. http://dx.doi.org/10.1007/978-1-4899-7504-1_24.

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Higgs, Michael J., E. Antonio Mangubat, Colin C. M. Moore, et al. "Case 174: Congenital Deformity." In Cosmetic Breast Cases. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-27714-1_52.

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Qin, Sihe, Lei Shi, Baofeng Guo, Shaofeng Jiao, and Jiancheng Zang. "Congenital Deformity of Lower Limbs." In Atlas of Limb Deformity. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-0999-1_2.

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Farr, Sebastian. "Sprengel Deformity." In Congenital and Acquired Deformities of the Pediatric Shoulder Girdle. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-81839-5_4.

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Shen, Ze-ren, Rui-yu Qing, and Jian-min Yao. "Repair of Congenital Eye Deformity." In Atlas of Cleft Lip and Palate & Facial Deformity Surgery. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-4419-4_14.

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Zhu, Yong-hong, and Jian-min Yao. "Repair of Congenital Nasal Deformity." In Atlas of Cleft Lip and Palate & Facial Deformity Surgery. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-4419-4_15.

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Conference papers on the topic "Congenital deformity"

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Tran, Tram, Susan Mahan, Samantha Spencer, James Kasser, and Collin May. "Prenatal Diagnosis of Congenital Lower Extremity Deformity." In Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.640.

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Davuluri, Sanjana, Taemin Oh, Kyrillos Akhnoukh, et al. "Complications Following Hemivertebrectomy for Congenital Scoliosis." In 28th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2024. http://dx.doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.58_2024.

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Introduction: Hemivertebrae are rare congenital anomalies that can cause severe scoliosis requiring surgical correction. We aimed to determine whether severity of deformities is associated with more long-term surgical complications following surgical correction. Methods: We performed a retrospective, single-institution review on patients who underwent hemivertebrectomy and spinal fusion for congenital scoliosis between 2008-2020. We extracted pertinent data on demographics, radiographic parameters, operative details, and complication rates. Subgroup analyses were also done by complication seve

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Ахмедова, Мехрибан Ахмедовна, and Елена Николаевна Щурова. "ANALYSIS OF THE CORRESPONDENCE OF THE FUNCTIONAL STATE OF ADOLESCENTS WITH SPINAL DEFORMITY OF VARIOUS ORIGINS." In Психология. Спорт. Здравоохранение: сборник избранных статей по материалам Международной научной конференции (Санкт-Петербург, Октябрь 2021). Crossref, 2021. http://dx.doi.org/10.37539/psm299.2021.43.96.007.

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Аналогичный характер изменений физиологических параметров, чувствительной и двигательной сфер у подростков с идиопатическим и врождённым сколиозом может свидетельствовать о том, что причиной наблюдаемых изменений является не этиология заболевания, а недостаточный уровень моторной активности и процессы, связанные с развитием деформации позвоночника. The similar nature of changes in physiological parameters, sensory and motor spheres in adolescents with idiopathic and congenital scoliosis may indicate that the cause of the observed changes is not the etiology of the disease, but an insufficient

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Горбач, Алина Павловна, Елена Николаевна Щурова, and Елена Николаевна Горбач. "STUDY OF VISUAL FEATURES OF THE SKIN OF THE BACK IN ADOLESCENTS WITH CONGENITAL SCOLIOSIS." In Фундаментальные и прикладные исследования. Актуальные проблемы и достижения: сборник статей всероссийской научной конференции (СанктПетербург, Октябрь 2022). Crossref, 2022. http://dx.doi.org/10.37539/1011.2022.36.93.007.

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При визуальном осмотре кожного покрова спины 17 детей и подростков с врожденным сколиозом в 65% наблюдений обнаруживались атрофические полосы, расширенные капилляры, неравномерная пигментация, атипичный рост волос; участки гипертрихоза; гиперпигментация кожи в проекции остистых отростков, выраженная венозная сеть. Обнаружены корреляции между величиной угла дуг и противодуг деформации позвоночного столба и количеством вариации патологических изменений кожи. Visual examination of the skin of the back of 17 children and adolescents with congenital scoliosis revealed atrophic stripes, dilated capi

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Kuhl, Spencer, Thomas M. Cook, Jose Morcuende, and Nicole Grosland. "Clubfoot Kickbar: Development of an Improved Brace for Use Following Correction of Clubfoot." In 2020 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/dmd2020-9043.

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Abstract The critical final phase of treatment for congenital talipes equinovarus, commonly referred to as clubfoot, using the Ponseti Method requires parents to use a brace in order to maintain the correct foot posture for 12–14 hours each night until four years of age. Parents have been vocal about a desire to allow their children some mobility while maintaining correct alignment for the treatment of this deformity. To that end, the University of Iowa’s medical device prototyping facility Protostudios utilizes 3D CAD design, rapid prototyping principles and state of the art 3D printers to qu

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Jhun, Choon-Sik, Mark B. Ratcliffe, and Julius M. Guccione. "Ventricular Wall Stress and Pump Function of Ventricular Septal Defect of Congenital Heart Defects." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206320.

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About 36,000 infants are born each year with a congenital heart defect (CHD) and charges for treatment surpass $2.2 billion for inpatient surgery alone. Of many different types of CHDs, ventricular septal defect (VSD) is the most common class (∼1/3 of CHDs) of heart deformity present at birth. Though many close spontaneously and rarely require treatment, VSD still accounts for ∼15% of defects requiring an invasive procedure within the first year of life [1]. Generally, the ventricular performance is indexed by geometry, shape, diastolic and systolic function, and myocardial contractility [2].

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Mahmoodian, Roza, and Sorin Siegler. "An MRI Based Study of Tarsal Development During Manipulation and Casting Therapy of Infant Clubfoot." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-42573.

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Ponseti technique is a common non-surgical treatment based on serial manipulation and casting for idiopathic infant clubfoot. We have used three dimensional MRI throughout the treatment, to investigate the effect of the casts on the clubfoot of a one week old (at the beginning of treatment) male with unilateral right idiopathic congenital clubfoot deformity. A total of 21 MRI scans were obtained during weekly serial manipulation and corrective casting. Changes in shape, volume, ossification, and positional relationships of the hind foot anlagen were studied. We found that immediate shape chang

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Zavalisca, Aurica, and Iuliana Gheorghian. "New trends in functional kyphoses recovery." In The International Scientific Congress "Sports. Olimpysm. Health". SOH 2023. 8th Edition. The State University of Physical Education and Sport, 2025. https://doi.org/10.52449/soh23.65.

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Kyphosis is an acquired or congenital deformity of the spine. It is the object of study of many scholars and specialists in the field. The recovery of kyphosis depends on the correction of all deviations from the normal, namely the deformation of the physiological curves of the spine, the head and neck tilted forward, the shoulder blades apart and separated from the ribcage, the shoulders brought forward, the chest sunken or in flexion, a deviation of vertebrae. Physiotherapy is constantly coming up with new ideas, programs and protocols, addressed to people diagnosed with functional kyphosis.

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Marchiori, Julia Gabriela Oliveira, Jennyfer Paulla Galdino Chaves, Maria Cecilia Closs Ono, and Adriana Keijiro Maeda. "Trigonocephaly associated with myelomeningocele in infant: Case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.040.

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Context: Trigonocephaly is a type of craniostenosis due to the early closure of the metopic suture. His diagnosis is eminently clinical, but imaging tests are essential. The recommended treatment is surgical and should preferably be performed at the age of 3 to 9 months. Association between craniosynostosis and neural tube defect (NTDs) is rare and was sometimes considered as mere coincidence. However, Martinez-Lage et al. hypothesize that there is a causal relationship between these malformations since myelomeningocele reduces intracranial pulse pressure, which stimulates the early closure of

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Reports on the topic "Congenital deformity"

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Zhu, Wenhao, Xing Ding, Jiale Zheng, et al. Characteristics, Treatment, and Research Development of Bertolotti’s Syndrome: A Bibliometric Analysis and Systematic Review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.1.0077.

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Review question / Objective: Bertolotti’s syndrome is a prevalent congenital deformity. However, many physicians fail to include it in their differential diagnosis for low back pain, which results in missed diagnosis or misdiagnosis. There is still a lack of standardized treatment and management strategies for Bertolotti’s syndrome. This study aimed to review the clinical characteristics and management of Bertolotti’s syndrome and reports bibliometric insights in advancements in Bertolotti’s syndrome research. Information sources: A thorough literature search of the PubMed, Embase, Medline, Sc

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