Spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol

Teive, Hélio Afonso Ghizoni; Munhoz, Renato P.; Ashizawa, Tetsuo

doi:10.1590/s0004-282x2011000600023

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“…Family history was positive for SCA10, including previously reported relatives (aunt and two cousins), whose symptoms were initially manifested during pregnancy 3 . Interestingly, this same family has also reported the occurrence of cerebellar symptoms triggered by ingestion of small amounts of alcohol, which was previously also published by the authors 4 .…”

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confidence: 69%

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

Moro

Munhoz

Raskin³

et al. 2013

Arq. Neuro-Psiquiatr.

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supporting

confidence: 69%

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

Moro

Munhoz

Raskin³

et al. 2013

Arq. Neuro-Psiquiatr.

Self Cite

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Spinocerebellar ataxias

Soong

Morrison

2018

Handbook of Clinical Neurology

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There are over 40 autosomal dominant spinocerebellar ataxias (SCAs) now identified. In this chapter we delineate the phenotypes of SCAs 1-44 and dentatorubral-pallidoluysian atrophy (DRPLA) and highlight the clinical and genetic features of the well characterised SCAs in detail in the main section of the chapter, along with their frequency and age at onset. We have included a section on the key phenotypic features of rare spinocerebellar ataxias and discuss rare and unusual presentations and genetic mechanisms of the ataxias and show differences between adult and paediatric presentations. We look at unusual mechanisms where knowledge is evolving in some dominant ataxias. For ease of reference we have tabulated historical aspects of the ataxias, major neurological diagnostic features, ataxias with predominant paediatric and infantile onset and list recognisable nerve conduction features. We comment on the anti-sense ataxia gene mechanisms and we discuss potential developments including exome sequencing and potential therapeutic options. A gene table listing all of the identified SCAs and DRPLA is also included with key references and gene locations and symbols with OMIM reference numbers for further reading.

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The preclinical stage of movement disorders

Eberhardt

Topka

2016

Basal Ganglia

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Spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol

Cited by 3 publications

References 2 publications

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

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

Spinocerebellar ataxias

The preclinical stage of movement disorders

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