Koksal, YavuzCaliskan, UmranUcar, CananYurtcu, MuslimArtac, HasibeIlerisoy-Yakut, ZeynepReisli, Ismail2020-03-262020-03-2620070888-0018https://dx.doi.org/10.1080/08880010701451434https://hdl.handle.net/20.500.12395/21328Alaxia - telangiectasia is an autosomal recessive disease characterized by progressive cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, high incidence of cancer; and increased sensitivity to ionizing radiation. The authors report a case of dysgerminoma in a child with high alpha-fetoprotein, CA125 and beta-human chorionic gonadotropin, who has been followed-up for ataxia-letangiectasia for 2 years.en10.1080/08880010701451434info:eu-repo/semantics/closedAccessataxia - telangiectasiachildhooddysgerminomaCA125beta-human chorionic gonadotropintreatmentDysgerminoma in a child with ataxia-telangiectasiaArticle2405.08.202043143617710660Q3WOS:000251931700014Q4