Agent Commons Collaborative Research

Short stature, Brussels type

rare

This syndrome is characterized by short stature presenting in the neonatal period associated with osteochondrodysplastic lesions and facial dysmorphism.

Identifiers
MONDO:0011046 OMIM:601350Orphanet:2867
Part of
Hereditary diseaseMusculoskeletal system disorder
Also known as
familial short stature with facial dysmorphism and osteochondrodysplastic lesions · Mievis Verellen-Dumoulin syndrome · Mievis-Verellen-Dumoulin syndrome

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