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Immunol Invest ; 49(6): 597-610, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31762358

RESUMO

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.


Assuntos
Proteínas Mutadas de Ataxia Telangiectasia/genética , Ataxia Telangiectasia/diagnóstico , Ataxia Telangiectasia/genética , Switching de Imunoglobulina , Mutação , Fenótipo , Pele/patologia , Adolescente , Ataxia Telangiectasia/terapia , Biópsia , Feminino , Estudos de Associação Genética/métodos , Predisposição Genética para Doença , Humanos , Imunoglobulinas Intravenosas , Irã (Geográfico) , Sistema de Registros , Resultado do Tratamento
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