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

Vaughan, David; Affendi, Adrinda; Sheahan, Patrick; Sweeney, Brian

Vaughan, David; Affendi, Adrinda; Sheahan, Patrick; Sweeney, Brian.

Affiliation

Vaughan D; Neurology, Cork University Hospital, Cork, Ireland davevau@gmail.com.
Affendi A; ORL-HNS, South Infirmary Victoria University Hospital, Cork, Ireland.
Sheahan P; ORL-HNS, South Infirmary Victoria University Hospital, Cork, Ireland.
Sweeney B; Neurology, Cork University Hospital Group, Cork, Ireland.

BMJ Case Rep ; 14(12)2021 Dec 30.

Article in En | MEDLINE | ID: mdl-34969792

Subject(s)

Spinocerebellar Ataxias; Vocal Cord Paralysis; Adult; Humans; Male; Mutation; Recurrent Laryngeal Nerve; Spinocerebellar Ataxias/complications; Spinocerebellar Ataxias/diagnostic imaging; Spinocerebellar Ataxias/genetics; Vocal Cord Paralysis/etiology

Key words

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

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Full text: 1 Database: MEDLINE Main subject: Vocal Cord Paralysis / Spinocerebellar Ataxias Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Year: 2021 Type: Article

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