Autosomal recessive Robinow syndrome

MONDO:0009999

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

Also known as: COVESDEM syndrome, RRS, Robinow syndrome, autosomal recessive, costovertebral segmentation defect-mesomelia syndrome, Covesdem syndrome, Covesdem syndrome, formerly, Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly, Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive Robinow syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive disease (994) ↑ Robinow syndrome (0)

Including sub-types (0) Tagged with Autosomal recessive Robinow syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.