Familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy

Erdemoglu A., AKBOSTANCI M. C., Selcuki D.

CLINICAL NEUROLOGY AND NEUROSURGERY, cilt.102, sa.3, ss.129-134, 2000 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 102 Sayı: 3
  • Basım Tarihi: 2000
  • Doi Numarası: 10.1016/s0303-8467(00)00077-9
  • Dergi Adı: CLINICAL NEUROLOGY AND NEUROSURGERY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.129-134
  • Anahtar Kelimeler: cerebellar ataxia, histopathology, hypogonadism, polyneuropathy, BOUCHER-NEUHAUSER SYNDROME, HYPOGONADOTROPIC HYPOGONADISM, SPINOCEREBELLAR ATAXIA, DEFICIENCY, DYSTROPHY
  • Ankara Üniversitesi Adresli: Evet

Özet

In this article, we report two siblings who have familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy documented by light microscopy. This combination has not been reported previously in the literature. Cerebellar ataxia and hypogonadism is reviewed according to the clinical and laboratory features of the reported cases in the literature. (C) 2000 Published by Elsevier Science B.V.