| Literature DB >> 31762358 |
Parisa Amirifar1,2, Reza Yazdani2, Tannaz Moeini Shad2, Alireza Ghanadan3, Hassan Abolhassani4, Martin Lavin5, Soheila Sotoudeh6, Asghar Aghamohammadi2.
Abstract
Ataxia-telangiectasia (A-T) is a rare autosomal recessive syndrome characterized by progressive cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency and cancer predisposition, caused by mutations in the ataxia telangiectasia mutated (ATM) gene. The clinical and immunological manifestations of A-T are very heterogeneous, especially at an early age, leading to frequent misdiagnosis. Cutaneous granulomas with unknown pathogenesis occur uncommonly in a minority of A-T patients. We herein report an unusual case of a 13-year-old girl with A-T who presented severe clinical manifestations, including multiple granulomatous lesions of the skin and a class switch defect phenotype. This patient is the first Iranian A-T case with cutaneous granulomatosis and immunodeficiency. In addition, the literature on skin granulomas in all previously reported A-T patients is reviewed indicating an increased frequency of elevated IgM level and female dominancy in this selected group of patients.Entities:
Keywords: ATM gene; Ataxia-Telangiectasia (A-T); Primary immunodeficiency; class switching defect (CSD); cutaneous granulomatosis
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Year: 2019 PMID: 31762358 DOI: 10.1080/08820139.2019.1692864
Source DB: PubMed Journal: Immunol Invest ISSN: 0882-0139 Impact factor: 3.657