Literature DB >> 454144

Hereditary cerebellar atrophy (Holmes type) with optic atrophy: a clinico-pathological study of four generations in a family.

H Budka, D Seemann, W Danielczyk.   

Abstract

A family with a dominantly inherited progressive cerebellar ataxia is described; four members of successive generations were affected. Neuropathological examination of one family member classified this disorder as hereditary cerebellar atrophy of Holmes type. An associated optic atrophy has not been previously reported in this disease.

Entities:  

Mesh:

Year:  1979        PMID: 454144     DOI: 10.1007/bf00342243

Source DB:  PubMed          Journal:  Arch Psychiatr Nervenkr (1970)


  11 in total

1.  [Unusual familial-hereditary disease of the central nervous system in a Lower Austrian family (with a contribution to comparative neuropathology of kuru)].

Authors:  F SEITELBERGER
Journal:  Wien Klin Wochenschr       Date:  1962-10-12       Impact factor: 1.704

2.  Familial cerebello-olivary degeneration with late development of rigidity and dementia.

Authors:  H R CARTER; C SUKAVAJANA
Journal:  Neurology       Date:  1956-12       Impact factor: 9.910

3.  Electroencephalographic changes in cerebellar degenerative lesions.

Authors:  L A LIVERSEDGE; V EMERY
Journal:  J Neurol Neurosurg Psychiatry       Date:  1961-11       Impact factor: 10.154

4.  [Not Available].

Authors:  L VAN BOGAERT
Journal:  J Belge Neurol Psychiatr       Date:  1947-05

5.  [2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy].

Authors:  Y Kato; K Takayama; Y Tsujiyama; T Kaga; H Satowa
Journal:  No To Shinkei       Date:  1970-10

6.  Hereditary disease of the cerebellar parenchyma.

Authors:  L P Weiner; B W Konigsmark
Journal:  Birth Defects Orig Artic Ser       Date:  1971-02

7.  Familial infantile cerebellar atrophy associated with retinal degeneration.

Authors:  S Carpenter; G A Schumacher
Journal:  Arch Neurol       Date:  1966-01

8.  Optic and cochleovestibular degenerations in the hereditary ataxias. I. Clinico-pathological and genetic aspects.

Authors:  L van Bogaert; L Martin
Journal:  Brain       Date:  1974-03       Impact factor: 13.501

9.  Late cortical cerebellar atrophy, a form of hereditary cerebellar ataxia.

Authors:  R B RICHTER
Journal:  Am J Hum Genet       Date:  1950-03       Impact factor: 11.025

10.  [EEG studies of spinocerebellar ataxia].

Authors:  G Sack; B Gruss; J Lössner; H Bachmann
Journal:  Psychiatr Neurol Med Psychol (Leipz)       Date:  1977-09
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.