Reference - PMID:19888300 - Coffin-Lowry syndrome.
Reference summary
- PubMed ID
- PMID:19888300
- Title
- Coffin-Lowry syndrome.
- Authors
- Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A
- Citation
- Eur J Hum Genet 2010 Jun;18(6):627-33
- Publication year
- 2010
- Abstract
- Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation, which is characterized in male patients by psychomotor and growth retardation and various skeletal anomalies. Typical facial changes and specific clinical and radiological signs in the hand are useful aids in the diagnosis. CLS is caused by mutations in the RPS6KA3 gene located at Xp22.2, which encodes RSK2, a growth-factor-regulated protein kinase. RPS6KA3 mutations are extremely heterogeneous and lead to loss of phosphotransferase activity in the RSK2 kinase, most often because of premature termination of translation.
