Literature DB >> 7191499

Presumably Azorean disease in a presumably non-Portuguese family.

E B Healton, J C Brust, D L Kerr, S Resor, A Penn.   

Abstract

Autosomal dominant motor system degeneration (ADMSD) is a hereditary ataxia that has been reported previously only in Portuguese families from the Azores Islands. Cerebellar ataxia, pyramidal and extrapyramidal signs, amyotrophy, dystonia, abnormal eye movements, and prominent eyes are variably present. Four members of a family had cerebellar ataxia, dystonic posturing, a variety of abnormal eye movements, and prominent eyes resulting from lid retraction. Eight other family members had a similar disease. The combination of cerebellar ataxia, dystonia, abnormal eye movements, and prominent eyes has been reported only in ADMSD. The family reported here may be the first example of ADMSD in a non-Portuguese family.

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Year:  1980        PMID: 7191499     DOI: 10.1212/wnl.30.10.1084

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  10 in total

Review 1.  Toward understanding Machado-Joseph disease.

Authors:  Maria do Carmo Costa; Henry L Paulson
Journal:  Prog Neurobiol       Date:  2011-11-23       Impact factor: 11.685

2.  A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease.

Authors:  A L DeStefano; L A Cupples; P Maciel; C Gaspar; J Radvany; D M Dawson; L Sudarsky; L Corwin; P Coutinho; P MacLeod
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

3.  Genetic aspects of autosomal dominant late onset cerebellar ataxia.

Authors:  A E Harding
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

Review 4.  Machado-Joseph disease in a Nigerian family: mutational origin and review of the literature.

Authors:  Shamsideen Abayomi Ogun; Sandra Martins; Philip B Adebayo; Clara O Dawodu; Jorge Sequeiros; Michael F Finkel
Journal:  Eur J Hum Genet       Date:  2014-04-30       Impact factor: 4.246

Review 5.  Mouse models of spinocerebellar ataxia type 3 (Machado-Joseph disease).

Authors:  Veronica F Colomer Gould
Journal:  Neurotherapeutics       Date:  2012-04       Impact factor: 7.620

6.  Characteristics of oculomotor disorders of a family with Joseph's disease.

Authors:  N Shimizu; Y Takiyama; Y Mizuno; M Mizuno; K Saito; M Yoshida
Journal:  J Neurol       Date:  1990-11       Impact factor: 4.849

7.  Delirium associated with Joseph disease.

Authors:  Y Fukutani; K Katsukawa; R Matsubara; K Kobayashi; I Nakamura; N Yamaguchi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-11       Impact factor: 10.154

8.  Brain stem atrophy in Joseph disease: a morphometric study using two-dimensional (area) measurement by computed tomography.

Authors:  Y Fukutani; K Katsukawa; Y Ishizaki; K Kobayashi; I Nakamura
Journal:  J Neurol       Date:  1991-07       Impact factor: 4.849

9.  Regional cerebral blood flow measured with N-isopropyl-p-[123I]iodoamphetamine single-photon emission tomography in patients with Joseph disease.

Authors:  N Takahashi; I Odano; M Nishihara; T Yuasa; K Sakai
Journal:  Eur J Nucl Med       Date:  1994-07

10.  The pathology of Machado-Joseph disease. Report of a possible homozygous case.

Authors:  P Coutinho; A Guimarães; F Scaravilli
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

  10 in total

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