Short stature syndrome, Brussels type

Alternate names[edit | edit source]

Familial short stature with facial dysmorphism and osteochondrodysplastic lesions; Mievis Verellen-Dumoulin syndrome

Definition[edit | edit source]

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

NIH genetic and rare disease info[edit source]

NIH info on Short stature syndrome, Brussels type

Short stature syndrome, Brussels type is a rare disease.

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Rare diseases - Short stature syndrome, Brussels type
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Also see	Comprehensive list of genetic and rare diseases
Resources	NIH GARD, US Genetic and Rare Diseases Info Rare Disease Day Undiagnosed Diseases Network Database of rare diseases at Orphanet Rare Disease UK Rare diseases search engine