200 top medical experts on Coffin-Lowry Syndrome across 12 countries and 9 U.S. states, including 13 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Coffin-Lowry Syndrome: 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): X-Linked Mental Retardation (2,803).
- Clinical Trials : at least 1 including 1 Completed
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