Clinical phenotype and functional analysis of a rare XIAP/BIRC4 mutation.

Klin Padiatr

Department of Pediatrics, UKSH, Campus Lübeck, Germany.

Published: November 2013

X-linked lymphoproliferative syndromes (XLP) are rare primary immunodeficiencies. Mutations within the XIAP/BIRC4 gene characterize XLP type 2 and cause XIAP deficiency. We present the case of a 5-year-old boy with a novel mutation of the XIAP/BIRC4 gene and describe the immunological phenotype for the first time. We characterized the distinct immunological phenotype and evaluated the family history accordingly.

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http://dx.doi.org/10.1055/s-0033-1355393DOI Listing

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