Catalog

Autosomal recessive Robinow syndrome

No MMS code

Link to WHO Definition

Autosomal recessive Robinow syndrome – http://id.who.int/icd/entity/793292660

Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.