Progeria short stature pigmented nevi: A very rare inherited disorder characterized by premature aging, short stature, and immune system deficiency. The type and severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Progeria short stature pigmented nevi is available below.
See full list of 26 symptoms of Progeria short stature pigmented nevi
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Progeria short stature pigmented nevi is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Progeria short stature pigmented nevi, or a subtype of Progeria short stature pigmented nevi,
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 Progeria short stature pigmented nevi as a "rare disease".
Source - Orphanet
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