Dominant omodysplasia—A sporadic case—A new case report and review of the literature

Omodysplasia is an extremely rare skeletal dysplasia. Since introducing this phenotype as a new syndrome, ten cases of the autosomal dominant type of this disease have been reported. Here, we present a new patient and review published articles in this field to provide a clinical diagnostic criterion...

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Detalles Bibliográficos
Autores principales: Arabzadeh, Aidin, Baghianimoghadam, Behnam, Nabian, Mohammad Hossein, Fallah, Yousef, Ebrahimnasab, Mohammad Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347672/
https://www.ncbi.nlm.nih.gov/pubmed/35937024
http://dx.doi.org/10.1002/ccr3.6187
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author Arabzadeh, Aidin
Baghianimoghadam, Behnam
Nabian, Mohammad Hossein
Fallah, Yousef
Ebrahimnasab, Mohammad Mehdi
author_facet Arabzadeh, Aidin
Baghianimoghadam, Behnam
Nabian, Mohammad Hossein
Fallah, Yousef
Ebrahimnasab, Mohammad Mehdi
author_sort Arabzadeh, Aidin
collection PubMed
description Omodysplasia is an extremely rare skeletal dysplasia. Since introducing this phenotype as a new syndrome, ten cases of the autosomal dominant type of this disease have been reported. Here, we present a new patient and review published articles in this field to provide a clinical diagnostic criterion.
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spelling pubmed-93476722022-08-05 Dominant omodysplasia—A sporadic case—A new case report and review of the literature Arabzadeh, Aidin Baghianimoghadam, Behnam Nabian, Mohammad Hossein Fallah, Yousef Ebrahimnasab, Mohammad Mehdi Clin Case Rep Case Report Omodysplasia is an extremely rare skeletal dysplasia. Since introducing this phenotype as a new syndrome, ten cases of the autosomal dominant type of this disease have been reported. Here, we present a new patient and review published articles in this field to provide a clinical diagnostic criterion. John Wiley and Sons Inc. 2022-08-03 /pmc/articles/PMC9347672/ /pubmed/35937024 http://dx.doi.org/10.1002/ccr3.6187 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Arabzadeh, Aidin
Baghianimoghadam, Behnam
Nabian, Mohammad Hossein
Fallah, Yousef
Ebrahimnasab, Mohammad Mehdi
Dominant omodysplasia—A sporadic case—A new case report and review of the literature
title Dominant omodysplasia—A sporadic case—A new case report and review of the literature
title_full Dominant omodysplasia—A sporadic case—A new case report and review of the literature
title_fullStr Dominant omodysplasia—A sporadic case—A new case report and review of the literature
title_full_unstemmed Dominant omodysplasia—A sporadic case—A new case report and review of the literature
title_short Dominant omodysplasia—A sporadic case—A new case report and review of the literature
title_sort dominant omodysplasia—a sporadic case—a new case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347672/
https://www.ncbi.nlm.nih.gov/pubmed/35937024
http://dx.doi.org/10.1002/ccr3.6187
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