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

David P VaughanAdrinda AffendiPatrick SheahanBrian Sweeney
Published in: BMJ case reports (2021)
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.
Keyphrases
  • intellectual disability
  • muscular dystrophy
  • case report
  • early onset
  • genome wide
  • genome wide identification
  • duchenne muscular dystrophy