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J Clin Immunol ; 35(1): 11-4, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25352054

ABSTRACT

Gain of function (GOF) mutation in the p110δ catalytic subunit of the phosphatidylinositol-3-OH kinase (PIK3CD) is the cause of a primary immunodeficiency (PID) characterized by recurrent sinopulmonary infections and lymphoproliferation. We describe a family of two adults and three children with GOF mutation in PIK3CD, all with recurrent sinopulmonary infections and varied infectious and non-infectious complications. The two adults have Primary Sclerosing Cholangitis (PSC) without evidence of Cryptosporidium parvum infection and have required liver transplantation. PSC is a novel phenotype of GOF mutation in PIK3CD.


Subject(s)
Cholangitis, Sclerosing/enzymology , Cholangitis, Sclerosing/genetics , Class I Phosphatidylinositol 3-Kinases/genetics , Mutation, Missense , Adult , Amino Acid Substitution , Child , Cholangitis, Sclerosing/immunology , Class I Phosphatidylinositol 3-Kinases/immunology , Class I Phosphatidylinositol 3-Kinases/metabolism , Female , Heterozygote , Humans , Immunologic Deficiency Syndromes/enzymology , Immunologic Deficiency Syndromes/genetics , Immunologic Deficiency Syndromes/immunology , Liver/pathology , Male , Pedigree
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