Deal-Barratt-Dillon syndrome: A very rare syndrome characterized mainly by scaly skin, jaundice, diarrhea and Fanconi syndrome (bone marrow fails to make sufficient new blood cells). More detailed information about the symptoms, causes, and treatments of Deal-Barratt-Dillon syndrome is available below.
See full list of 13 symptoms of Deal-Barratt-Dillon syndrome
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Read more about Misdiagnosis and Deal-Barratt-Dillon syndrome
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Prognosis for Deal-Barratt-Dillon syndrome: infant death
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Types of Deal-Barratt-Dillon syndrome
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Deal-Barratt-Dillon syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Deal-Barratt-Dillon syndrome, or a subtype of Deal-Barratt-Dillon 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 Deal-Barratt-Dillon syndrome as a "rare disease".
Source - Orphanet
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