Inherited defects in adenosine deaminase (ADA) cause a subtype of severe combined immunodeficiency (SCID), known as ADA-SCID. Most affected infants can be diagnosed while still asymptomatic by a SCID newborn screening test, allowing early initiation of therapy. We reviewed the evidence currently available and propose a consensus management strategy. In addition to the treatment of the immune deficiency of ADA-SCID, patients should be followed for specific non-infectious respiratory, neurological and biochemical complications associated with ADA deficiency. (Source: Journal of Allergy and Clinical Immunology)
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Τετάρτη 5 Σεπτεμβρίου 2018
Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency
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