Dysgerminoma in a child with ataxia-telangiectasia
Küçük Resim Yok
Tarih
2007
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
TAYLOR & FRANCIS INC
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Alaxia - 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.
Açıklama
Anahtar Kelimeler
ataxia - telangiectasia, childhood, dysgerminoma, CA125, beta-human chorionic gonadotropin, treatment
Kaynak
PEDIATRIC HEMATOLOGY AND ONCOLOGY
WoS Q Değeri
Q4
Scopus Q Değeri
Q3
Cilt
24
Sayı
05.08.2020
