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Ptosis and bulbar onset: an unusual phenotype of familial ALS?

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

Abstract

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder of upper and lower motor neurons that usually spare the oculomotor nerves. Here, we describe a case of two siblings with a familial bulbar-onset ALS both with ptosis manifested at the onset of the disease.
Original languageEnglish
Pages (from-to)377-378
JournalNeurological Sciences
Volume39
Issue number2
DOIs
Publication statusPublished - 2018

Keywords

  • Amyotrophic lateral sclerosis
  • Familial cases
  • Motor neuron disease
  • Ptosis

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