Burnett-Schwartz-Berberian syndrome: A rare syndrome characterized by an inflammatory facial skin disorder and various congenital anomalies. More detailed information about the symptoms, causes, and treatments of Burnett-Schwartz-Berberian syndrome is available below.
See full list of 10 symptoms of Burnett-Schwartz-Berberian syndrome
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Types of Burnett-Schwartz-Berberian syndrome
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Burnett-Schwartz-Berberian syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Burnett-Schwartz-Berberian syndrome, or a subtype of Burnett-Schwartz-Berberian 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 Burnett-Schwartz-Berberian syndrome as a "rare disease".
Source - Orphanet
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