Category:Robinow syndrome

**Robinow syndrome**
	syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities
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Instance of	rare disease; class of disease;
Subclass of	syndrome; autosomal genetic disease;
Named after	Meinhard Robinow;
Discoverer or inventor	Meinhard Robinow; Frederic N. Silverman;
Authority file
	Q1475743;
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Media in category "Robinow syndrome"

The following 7 files are in this category, out of 7 total.