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GCS1 (medical condition): A rare syndrome characterized mainly by retarded fetal...more »
GCS1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that GCS1, or a subtype of GCS1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
GCS1: Another name for Camptodactyly syndrome, Guadalajara type 1 (or close medical condition association).
»Introduction: Camptodactyly syndrome, Guadalajara type 1
»Symptoms of Camptodactyly syndrome, Guadalajara type 1
GCS1: GCS1 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of GCS1 incude:
Source - NIH
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