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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Bibliographic Details
Published in:Clinical case reports 2022-08, Vol.10 (8), p.e6187-n/a
Main Authors: Arabzadeh, Aidin, Baghianimoghadam, Behnam, Nabian, Mohammad Hossein, Fallah, Yousef, Ebrahimnasab, Mohammad Mehdi
Format: Article
Language:English
Subjects:
Case Report
Case reports
criteria
diagnosis
dominant omodysplasia
Elbow
Mutation
Nose
Patients
Radiography
Surgery
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Summary: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.
ISSN:2050-0904
2050-0904
DOI:10.1002/ccr3.6187