De Sanctis-Cacchione syndrome: A rare genetic ectodermal disorder characterized by sunlight sensitivity, skin atrophy and pigmentation and skin tumors as well asneurologic involvement. More detailed information about the symptoms, causes, and treatments of De Sanctis-Cacchione syndrome is available below.
See full list of 50 symptoms of De Sanctis-Cacchione syndrome
Review possible medical complications related to De Sanctis-Cacchione syndrome:
Research the causes of these diseases that are similar to, or related to, De Sanctis-Cacchione syndrome:
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Medical research articles related to De Sanctis-Cacchione syndrome include:
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De Sanctis-Cacchione syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that De Sanctis-Cacchione syndrome, or a subtype of De Sanctis-Cacchione 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 De Sanctis-Cacchione syndrome as a "rare disease".
Source - Orphanet
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