Early onset hereditary ataxias of unknown etiology. Review of a personal series

Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):420-30.

Abstract

Among 300 patients affected by hereditary ataxia, 94 received the diagnosis of Friedreich's disease, 12 of Late Onset Friedreich's disease, 27 of Early Onset Cerebellar Ataxia with retained tendon reflexes, 10 of Progressive Myoclonic Ataxia, 4 of Ataxia with hypogonadism and 2 of Ataxia with hearing loss. Only Friedreich's disease appears clinically homogeneous, whereas the others are not specific entities and each of them probably includes different diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Ataxia / classification
  • Ataxia / complications
  • Ataxia / genetics*
  • Ataxia / physiopathology
  • Cerebellar Ataxia / epidemiology
  • Cerebellar Ataxia / genetics
  • Child
  • Child, Preschool
  • Diabetes Complications
  • Female
  • Friedreich Ataxia / classification
  • Friedreich Ataxia / diagnosis
  • Friedreich Ataxia / genetics
  • Hearing Loss, Sensorineural / complications
  • Humans
  • Hypogonadism / complications
  • Infant
  • Infant, Newborn
  • Male
  • Middle Aged
  • Myoclonic Cerebellar Dyssynergia / diagnosis
  • Myoclonic Cerebellar Dyssynergia / genetics
  • Neural Conduction
  • Prevalence