Camptodactyly syndrome, Guadalajara type 1: A rare syndrome characterized mainly by retarded fetal growth and permanently flexed fingers as well as other abnormalities such as short toes, short neck and a small head. More detailed information about the symptoms, causes, and treatments of Camptodactyly syndrome, Guadalajara type 1 is available below.
See full list of 22 symptoms of Camptodactyly syndrome, Guadalajara type 1
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Camptodactyly syndrome, Guadalajara type 1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Camptodactyly syndrome, Guadalajara type 1, or a subtype of Camptodactyly syndrome, Guadalajara type 1,
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 it affects 1 person per 2,000.
They list Camptodactyly syndrome, Guadalajara type 1 as a "rare disease".
Source - Orphanet
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