Literature DB >> 21236683

Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium.

H A G Teive1, W O Arruda, S Raskin, R P Munhoz, J A Zavala, L C Werneck, T Ashizawa.   

Abstract

Spinocerebellar ataxia type 10 is an autosomal dominant neurodegenerative disorder. It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms. The authors report three patients from the same family who were asymptomatic until gestation and puerperium, when they developed symptoms and signs suggestive of the syndrome. Genetic diagnosis was made in the three patients. The authors hypothesize that hormonal changes are likely to influence the manifestation of the condition.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21236683     DOI: 10.1016/j.jocn.2010.07.102

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  3 in total

1.  Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids.

Authors:  Adriana Moro; Renato P Munhoz; Salmo Raskin; Torben C Bezerra; Mariana Moscovich; Tetsuo Ashizawa; Hélio A G Teive
Journal:  Arq Neuropsiquiatr       Date:  2013-01       Impact factor: 1.420

2.  Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.

Authors:  Hélio A G Teive; Renato P Munhoz; Walter O Arruda; Iscia Lopes-Cendes; Salmo Raskin; Lineu C Werneck; Tetsuo Ashizawa
Journal:  Clinics (Sao Paulo)       Date:  2012       Impact factor: 2.365

3.  A refractory head tremor appearing after volatile anesthesia combined with epidural anesthesia in a patient with spinocerebellar ataxia type 6.

Authors:  Takaya Nishida; Masayori Nakajima
Journal:  JA Clin Rep       Date:  2018-01-30
  3 in total

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