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Oculo-facio-cardio-dental syndrome in a girl and her mother

Congenital heart defects are known to be associated with facial dysmorphism and other congenital anomalies. Oculo-facio-cardio-dental (OFCD) syndrome is one such rare multiple congenital anomaly syndrome inherited as an X-linked dominant condition characterized by congenital cataracts, multiple mino...

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Detalles Bibliográficos
Autores principales: Rudrappa, Sudha, Kumar, Rajendra, Kumar, G. S.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009431/
https://www.ncbi.nlm.nih.gov/pubmed/21206708
http://dx.doi.org/10.4103/0971-6866.73416
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author Rudrappa, Sudha
Kumar, Rajendra
Kumar, G. S.
author_facet Rudrappa, Sudha
Kumar, Rajendra
Kumar, G. S.
author_sort Rudrappa, Sudha
collection PubMed
description Congenital heart defects are known to be associated with facial dysmorphism and other congenital anomalies. Oculo-facio-cardio-dental (OFCD) syndrome is one such rare multiple congenital anomaly syndrome inherited as an X-linked dominant condition characterized by congenital cataracts, multiple minor facial dysmorphic features, congenital heart defects and dental anomalies. It is unrecognized by many medical and dental professionals. Only 21 cases have been reported so far. This syndrome is often misrecognized as rubella embryopathy because of association of congenital cataract with cardiac anomalies. It is usually the orthodontists who diagnose the syndrome based on typical findings on dental panoramic radiographs. But we suspected our patient to be having OFCD syndrome based on typical facial dysmorphism, ocular and cardiac defects, and finally it was confirmed after noticing typical dental radiographic findings.
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spelling pubmed-30094312011-01-04 Oculo-facio-cardio-dental syndrome in a girl and her mother Rudrappa, Sudha Kumar, Rajendra Kumar, G. S. Indian J Hum Genet Case Report Congenital heart defects are known to be associated with facial dysmorphism and other congenital anomalies. Oculo-facio-cardio-dental (OFCD) syndrome is one such rare multiple congenital anomaly syndrome inherited as an X-linked dominant condition characterized by congenital cataracts, multiple minor facial dysmorphic features, congenital heart defects and dental anomalies. It is unrecognized by many medical and dental professionals. Only 21 cases have been reported so far. This syndrome is often misrecognized as rubella embryopathy because of association of congenital cataract with cardiac anomalies. It is usually the orthodontists who diagnose the syndrome based on typical findings on dental panoramic radiographs. But we suspected our patient to be having OFCD syndrome based on typical facial dysmorphism, ocular and cardiac defects, and finally it was confirmed after noticing typical dental radiographic findings. Medknow Publications 2010 /pmc/articles/PMC3009431/ /pubmed/21206708 http://dx.doi.org/10.4103/0971-6866.73416 Text en © Indian Journal of Human Genetics http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rudrappa, Sudha
Kumar, Rajendra
Kumar, G. S.
Oculo-facio-cardio-dental syndrome in a girl and her mother
title Oculo-facio-cardio-dental syndrome in a girl and her mother
title_full Oculo-facio-cardio-dental syndrome in a girl and her mother
title_fullStr Oculo-facio-cardio-dental syndrome in a girl and her mother
title_full_unstemmed Oculo-facio-cardio-dental syndrome in a girl and her mother
title_short Oculo-facio-cardio-dental syndrome in a girl and her mother
title_sort oculo-facio-cardio-dental syndrome in a girl and her mother
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009431/
https://www.ncbi.nlm.nih.gov/pubmed/21206708
http://dx.doi.org/10.4103/0971-6866.73416
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