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Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East

INTRODUCTION: Chondroectodermal dysplasia (Ellis–van Creveld syndrome (EVC)) (OMIM: #225500) is a rare skeletal dysplasia with unknown exact prevalence. EVC patients may have abnormal skeletal and extra skeletal symptoms. We report a case of EVC patient and review previous cases reported in Iran. MA...

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Autores principales: Baghianimoghadam, Behnam, Arabzadeh, Aidin, Fallah, Yousef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Vilnius University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958661/
https://www.ncbi.nlm.nih.gov/pubmed/35474936
http://dx.doi.org/10.15388/Amed.2021.28.2.11
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author Baghianimoghadam, Behnam
Arabzadeh, Aidin
Fallah, Yousef
author_facet Baghianimoghadam, Behnam
Arabzadeh, Aidin
Fallah, Yousef
author_sort Baghianimoghadam, Behnam
collection PubMed
description INTRODUCTION: Chondroectodermal dysplasia (Ellis–van Creveld syndrome (EVC)) (OMIM: #225500) is a rare skeletal dysplasia with unknown exact prevalence. EVC patients may have abnormal skeletal and extra skeletal symptoms. We report a case of EVC patient and review previous cases reported in Iran. MATERIALS AND METHODS: The patient was a 30 years old woman referred to our hand clinic for an extra finger in both hands. She was born to a consanguineous marriage. The patient had a history of bilateral valgus deformity of the knees, for which she underwent proximal tibial and distal femoral osteotomy. Upon examination, the patient had bilateral polydactyly and brachymetacarpia with hypotrophic fingernails. She was about 120 cm tall and had acromesomelic type dwarfism. Oral examination revealed serrated incisal margins, dental transposition, a diastema, conical teeth and, enamel hypoplasia. In the radiographic examination of upper extremity, postaxial polydactyly and polymetacarpia, enlarged distal radius, and fusion of capitate and hamate were seen. We searched online databases (Pubmed, Scopus, Google Scholar) and found 14 Iranian papers with 21 reported patients (there was no time limit). We reviewed available clinical and genetic data and the geographic origins of patients. RESULTS: 14 articles reporting 22 EVC patients (including our patient) from Iran have been published in Persian and English (7 in Persian and 7 in English). All patients presented with characteristic EVC symptoms but were diagnosed at a relatively late age, 18 patients were born to consanguineous marriages CONCLUSIONS: It seems that based on these studies, it is possible to identify some families with this genetic mutation. We can warn such families of the dangers of consanguineous marriage through genetic counseling before marriage. In addition, by identifying families with such problems, we can detect such anomalies in the baby earlier with more careful prenatal care.
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spelling pubmed-89586612022-04-25 Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East Baghianimoghadam, Behnam Arabzadeh, Aidin Fallah, Yousef Acta Med Litu Case Studies INTRODUCTION: Chondroectodermal dysplasia (Ellis–van Creveld syndrome (EVC)) (OMIM: #225500) is a rare skeletal dysplasia with unknown exact prevalence. EVC patients may have abnormal skeletal and extra skeletal symptoms. We report a case of EVC patient and review previous cases reported in Iran. MATERIALS AND METHODS: The patient was a 30 years old woman referred to our hand clinic for an extra finger in both hands. She was born to a consanguineous marriage. The patient had a history of bilateral valgus deformity of the knees, for which she underwent proximal tibial and distal femoral osteotomy. Upon examination, the patient had bilateral polydactyly and brachymetacarpia with hypotrophic fingernails. She was about 120 cm tall and had acromesomelic type dwarfism. Oral examination revealed serrated incisal margins, dental transposition, a diastema, conical teeth and, enamel hypoplasia. In the radiographic examination of upper extremity, postaxial polydactyly and polymetacarpia, enlarged distal radius, and fusion of capitate and hamate were seen. We searched online databases (Pubmed, Scopus, Google Scholar) and found 14 Iranian papers with 21 reported patients (there was no time limit). We reviewed available clinical and genetic data and the geographic origins of patients. RESULTS: 14 articles reporting 22 EVC patients (including our patient) from Iran have been published in Persian and English (7 in Persian and 7 in English). All patients presented with characteristic EVC symptoms but were diagnosed at a relatively late age, 18 patients were born to consanguineous marriages CONCLUSIONS: It seems that based on these studies, it is possible to identify some families with this genetic mutation. We can warn such families of the dangers of consanguineous marriage through genetic counseling before marriage. In addition, by identifying families with such problems, we can detect such anomalies in the baby earlier with more careful prenatal care. Vilnius University Press 2021 2021-08-20 /pmc/articles/PMC8958661/ /pubmed/35474936 http://dx.doi.org/10.15388/Amed.2021.28.2.11 Text en Copyright © 2021 Behnam Baghianimoghadam, Aidin Arabzadeh, Yousef Fallah. https://creativecommons.org/licenses/by/4.0/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 author and source are credited.
spellingShingle Case Studies
Baghianimoghadam, Behnam
Arabzadeh, Aidin
Fallah, Yousef
Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
title Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
title_full Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
title_fullStr Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
title_full_unstemmed Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
title_short Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
title_sort ellis–van creveld syndrome in iran, a case report and review of disease cases in iran, middle east
topic Case Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958661/
https://www.ncbi.nlm.nih.gov/pubmed/35474936
http://dx.doi.org/10.15388/Amed.2021.28.2.11
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