Vocal cord paralysis as a presenting sign of autosomal recessive spinocerebellar atrophy type 10

David Vaughan; Adrinda Affendi; Patrick Sheahan; Brian Sweeney

doi:10.1136/bcr-2021-245484

Vocal cord paralysis as a presenting sign of autosomal recessive spinocerebellar atrophy type 10

David Vaughan
, Adrinda Affendi
, Patrick Sheahan
, Brian Sweeney

School of Medicine

Research output: Contribution to journal › Article › peer-review

Abstract

Acquired vocal cord paralysis (VCP) is caused by dysfunction or injury of one or both recurrent laryngeal nerves. Here we report a 41-year-old man with spinocerebellar atrophy, autosomal recessive type 10 (SCAR10) due to an autosomal recessive mutation in the ANO10 gene, with VCP as the presenting symptom. He later developed ataxia and speech disturbance.

Original language	English
Article number	e245484
Journal	BMJ Case Reports
Volume	14
Issue number	12
DOIs	https://doi.org/10.1136/bcr-2021-245484
Publication status	Published - 30 Dec 2021

Keywords

brain stem / cerebellum
genetic screening / counselling
neuro genetics
neurology
otolaryngology / ENT

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10.1136/bcr-2021-245484

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abstract = "Acquired vocal cord paralysis (VCP) is caused by dysfunction or injury of one or both recurrent laryngeal nerves. Here we report a 41-year-old man with spinocerebellar atrophy, autosomal recessive type 10 (SCAR10) due to an autosomal recessive mutation in the ANO10 gene, with VCP as the presenting symptom. He later developed ataxia and speech disturbance.",

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N2 - Acquired vocal cord paralysis (VCP) is caused by dysfunction or injury of one or both recurrent laryngeal nerves. Here we report a 41-year-old man with spinocerebellar atrophy, autosomal recessive type 10 (SCAR10) due to an autosomal recessive mutation in the ANO10 gene, with VCP as the presenting symptom. He later developed ataxia and speech disturbance.

AB - Acquired vocal cord paralysis (VCP) is caused by dysfunction or injury of one or both recurrent laryngeal nerves. Here we report a 41-year-old man with spinocerebellar atrophy, autosomal recessive type 10 (SCAR10) due to an autosomal recessive mutation in the ANO10 gene, with VCP as the presenting symptom. He later developed ataxia and speech disturbance.

KW - brain stem / cerebellum

KW - genetic screening / counselling

KW - neuro genetics

KW - neurology

KW - otolaryngology / ENT

UR - https://www.scopus.com/pages/publications/85122575047

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M3 - Article

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ER -

Vocal cord paralysis as a presenting sign of autosomal recessive spinocerebellar atrophy type 10

Abstract

Keywords

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