Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID) |
| |
Authors: | Kühl J S Schwarz K Münch A Schmugge M Pekrun A Meisel C Wahn V Ebell W von Bernuth H |
| |
Affiliation: | University Hospital Berlin, Department for Pediatric Hematology and Oncology, Berlin, Germany. |
| |
Abstract: | ![]() Adenosin deaminase (ADA) deficiency is the cause for Severe Combined Immunodeficiency (SCID) in about 15% of patients with SCID, often presenting as T (-)B (-)NK (-)SCID. Treatment options for ADA-SCID are enzyme replacement, bone marrow transplantation or gene therapy. We here describe the first patient with ADA-SCID and fatal hepatic failure despite bone marrow transplantation from a 10/10 HLA identical related donor. As patients with ADA-SCID may be at yet underestimated increased risk for rapid hepatic failure we speculate whether hepatitis in ADA-SCID should lead to the immediate treatment with enzyme replacement by pegylated ADA. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|