Autosomal recessive Robinow syndrome

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Name:
Autosomal recessive Robinow syndrome
Description:
Autosomal recessive Robinow syndrome (RRS) is the less common type of Robinow syndrome (RS, see this term) characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.
ORPHAcode:
1507
Synonyms:
COVESDEM syndrome
Costovertebral segmentation defect-mesomelia syndrome
RRS
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14