Hutchinson Gilford Syndrome: A rare genetic disorder characterized by alopecia and senile-like appearance. More detailed information about the symptoms, causes, and treatments of Hutchinson Gilford Syndrome is available below.
See full list of 32 symptoms of Hutchinson Gilford Syndrome
Review possible medical complications related to Hutchinson Gilford Syndrome:
See full list of 7 occasional symptoms of Hutchinson Gilford Syndrome
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Hutchinson Gilford Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hutchinson Gilford Syndrome, or a subtype of Hutchinson Gilford 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 Hutchinson Gilford Syndrome as a "rare disease".
Source - Orphanet
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