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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