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

Abstract

Abstract 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.

Keywords

• criteria
• diagnosis
• dominant omodysplasia