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Coffin syndrome (medical condition): A rare genetic disorder characterized by down...more »
These medical condition or symptom topics may be relevant to medical information for Coffin syndrome:
Coffin syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Coffin syndrome, or a subtype of Coffin syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Coffin syndrome as a "rare disease".
Source - Orphanet
Coffin syndrome: Another name for Coffin-Lowry syndrome (or close medical condition association).
»Introduction: Coffin-Lowry syndrome
»Symptoms of Coffin-Lowry syndrome
»Treatments for Coffin-Lowry syndrome
Coffin syndrome: Coffin syndrome is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Coffin syndrome incude:
Treatments for Coffin syndrome (Coffin-Lowry syndrome) include:
Treatment of Coffin syndrome: For more treatment information about Coffin syndrome, see treatment of Coffin-Lowry syndrome (Coffin syndrome)
Coffin-Lowry syndrome is a rare genetic disorder characterized by craniofacial (head and facial) and skeletal ... (Source: excerpt from NINDS Coffin Lowry Information Page: NINDS)
These medical disease topics may be related to Coffin syndrome:
Source - NIH
Search to find out more about Coffin syndrome:
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