Introduction: Coffin-Lowry syndrome


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Coffin-Lowry syndrome: Rare genetic condition causing various abnormalities.

Coffin-Lowry syndrome: Coffin-Lowry syndrome is a rare genetic disorder characterized by craniofacial (head and facial) and skeletal abnormalities, mental retardation, short stature, and hypotonia. 1

Researching symptoms of Coffin-Lowry syndrome: Further information about the symptoms of Coffin-Lowry syndrome is available including a list of symptoms of Coffin-Lowry syndrome, or alternatively return to research other symptoms in the symptom center.

Treatments for Coffin-Lowry syndrome: Various information is available about treatments available for Coffin-Lowry syndrome, or research treatments for other diseases.

Causes of Coffin-Lowry syndrome: Research more detailed information about the causes of Coffin-Lowry syndrome, or other general information about Coffin-Lowry syndrome.

Statistics and Coffin-Lowry syndrome: Various sources and calculations are available in statistics about Coffin-Lowry syndrome, prevalence and incidence statistics for Coffin-Lowry syndrome, and you can also research other medical statistics in our statistics center.

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Footnotes:
1. excerpt from NINDS Coffin Lowry Information Page: NINDS

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