The investigated case of etiology of chylous pleural effusion: Ataxia-telangiectasia

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dc.contributor.authorSak, I
dc.contributor.authorKizilirmak, D
dc.contributor.authorHavlucu, Y
dc.contributor.authorYilmaz, Z
dc.contributor.authorÇelik, P
dc.date.accessioned2025-04-10T10:31:26Z
dc.date.available2025-04-10T10:31:26Z
dc.description.abstractAtaxia-telangiectasia is an autosomal recessive, rare, neurodegenerative multisystem disorder characterized by ataxia-telangiectasia, cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, progressive respiratory failure associated with increased malignancy risk. Clinical diagnosis is made with ataxia-telangiectasia mutated (ATM) gene. Our case, who was diagnosed as ataxia-telangiectasia while investigating the etiology of chylous pleural effusion, is presented because of its rare occurrence.
dc.identifier.issn0494-1373
dc.identifier.urihttp://hdl.handle.net/20.500.14701/37954
dc.language.isoEnglish
dc.titleThe investigated case of etiology of chylous pleural effusion: Ataxia-telangiectasia
dc.typeArticle

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