Coffin-Lowry Syndrome
MESHD038921
A rare, X-linked INTELLECTUAL DISABILITY syndrome that results from mutations in the RIBOSOMAL PROTEIN S6 KINASE gene. Typical manifestations of the disease include an intelligence quotient of less than 50, facial anomalies, and other malformations.
Synonyms
- Coffin Lowry Syndrome
- Syndrome, Coffin-Lowry
- Mental Retardation with Osteocartilaginous Abnormalities
- Coffin Syndrome
- Syndrome, Coffin
Source last updated 2026-05-24T15:25:13.889Z