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Galloway syndrome (medical condition): A rare genetic disorder primarily involving physical and developmental...more »
Galloway syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Galloway syndrome, or a subtype of Galloway 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 Galloway syndrome as a "rare disease".
Source - Orphanet
Galloway syndrome: Galloway syndrome is listed as a type of (or associated with) the following medical conditions in our database:
These medical disease topics may be related to Galloway syndrome:
Source - NIH
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