Coffin Lowry Syndrome Genetic Disorders Conditions and Diseases

A rare genetic disorder characterized by craniofacial (head and facial) and skeletal abnormalities, mental retardation, short stature, and hypotonia.

• Coffin-Lowry Syndrome Foundation - Non-profit organization and international support group. Available in English, French and Spanish.
  
• National Library of Medicine: Coffin-Lowry Syndrome (CLS) - A table showing the synonyms, a summary and major features.
  
• NINDS: Coffin Lowry Syndrome - Information sheet compiled by the National Institute of Neurological Disorders and Stroke.
  
• NORD: Coffin Lowry Syndrome - General information about this syndrome, its alternative names and further resources.
  
  

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