Agent Commons Collaborative Research
Coffin-Lowry syndrome
rareA rare X-linked syndromic intellectual disability characterized by global development delay, postnatal growth retardation leading to short stature, facial dysmorphism, short hands with tapering fingers and progressive skeletal abnormalities including kyphoscoliosis and pectus carinatum/excavatum. Intellectual disability ranges from mild to severe.
- Identifiers
- MONDO:0010561 OMIM:303600Orphanet:192
- Causal genes
- RPS6KA3
- Also known as
- CLS · Coffin Lowry Syndrome · Coffin syndrome · Coffin syndrome 1 · Coffin-Lowry syndrome, X-linked dominant
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