De Vaal syndrome
De Vaal syndrome: Introduction
De Vaal syndrome: A rare condition characterized by the defective development of T-cells, B-cells, thrombocytes and granulocytes. Severe immunodeficiency results which leads to infant death unless a bone marrow transplant is performed.
More detailed information about the symptoms,
causes, and treatments of De Vaal syndrome is available below.
Symptoms of De Vaal syndrome
See full list of 9
symptoms of De Vaal syndrome
De Vaal syndrome: Complications
Review possible medical complications related to De Vaal syndrome:
Medical Textbooks Online about De Vaal syndrome
Medical Books Excerpts
- LEUCOPENIA
- "Algorithmic Diagnosis of Symptoms and Signs" (2003)
- [ read ]
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Wrongly Diagnosed with De Vaal syndrome?
Causes of De Vaal syndrome
Read more about causes of De Vaal syndrome.
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Definitions of De Vaal syndrome:
De Vaal 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 Vaal syndrome, or a subtype of De Vaal 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 Vaal syndrome as a "rare disease".
Source - Orphanet
Contents for De Vaal syndrome:
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