Literature DB >> 7871993

Kabuki make-up syndrome associated with chronic idiopathic thrombocytopenic purpura.

T Watanabe1, M Miyakawa, M Satoh, T Abe, Y Oda.   

Abstract

Although susceptibility to infections in Kabuki make-up syndrome (KMS) has frequently been reported, there have been few immunological studies. We describe a 14 year old girl with KMS exhibiting chronic idiopathic thrombocytopenic purpura (chronic ITP), including immunological studies. Corticosteroid therapy was not effective therefore splenectomy was performed. The patient's platelet count increased transiently. Immunological studies revealed normal T cell functions and low serum immunoglobulin A (IgA) levels. Because of the abnormalities of B cell functions in chronic ITP and low serum IgA levels in our patient, we speculate that there may be some abnormalities of humoral immunity in KMS.

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Year:  1994        PMID: 7871993     DOI: 10.1111/j.1442-200x.1994.tb03281.x

Source DB:  PubMed          Journal:  Acta Paediatr Jpn        ISSN: 0374-5600


  2 in total

Review 1.  Epigenetic control of the immune system: a lesson from Kabuki syndrome.

Authors:  Stefano Stagi; Anna Virginia Gulino; Elisabetta Lapi; Donato Rigante
Journal:  Immunol Res       Date:  2016-04       Impact factor: 2.829

2.  Cardiac conduction abnormalities and congenital immunodeficiency in a child with Kabuki syndrome: case report.

Authors:  Maulik Shah; Brian Bogucki; Melissa Mavers; Daphne E deMello; Alan Knutsen
Journal:  BMC Med Genet       Date:  2005-07-25       Impact factor: 2.103

  2 in total

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