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ADA Deficiency: Adenosine deaminase deficiency is a condition which is inherited that results severe combined immunodeficiency disease. More detailed information about the symptoms, causes, and treatments of ADA Deficiency is available below.
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Read more about complications of ADA Deficiency.
Research the causes of these diseases that are similar to, or related to, ADA Deficiency:
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Read more about Misdiagnosis and ADA Deficiency
Medical research articles related to ADA Deficiency include:
Click here to find more evidence-based articles on the TRIP Database
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Visit our research pages for current research about ADA Deficiency treatments.
Types of ADA Deficiency
Read about other experiences, ask a question about ADA Deficiency, or answer someone else's question, on our message boards:
An autosomal recessive deficiency of the purine salvage enzyme adenosine deaminase which results in Severe Combined Immunodeficiency Disease (SCID). The most common form of SCID, accounting for about 50% of autosomal recessive cases. The first disease for which gene therapy was applied. - (Source - Diseases Database)
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