Verloes Gillerot Fryns syndrome: A syndrome characterised by multiple congenital abnormalities and mental retardation. More detailed information about the symptoms, causes, and treatments of Verloes Gillerot Fryns syndrome is available below.
See full list of 10 symptoms of Verloes Gillerot Fryns syndrome
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Verloes Gillerot Fryns syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Verloes Gillerot Fryns syndrome, or a subtype of Verloes Gillerot Fryns 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 it affects 1 person per 2,000.
They list Verloes Gillerot Fryns syndrome as a "rare disease".
Source - Orphanet
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