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Gyrate atrophy (medical condition): Excessive levels of ornithine in the blood caused by a...more »
Gyrate atrophy: Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Gyrate atrophy:
Gyrate atrophy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Gyrate atrophy, or a subtype of Gyrate atrophy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Gyrate atrophy: Gyrate atrophy is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Gyrate atrophy incude:
These medical disease topics may be related to Gyrate atrophy:
The following list attempts to classify Gyrate atrophy into categories where each line is subset of the next.
Search to find out more about Gyrate atrophy:
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