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

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer 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.
Lingua originaleInglese
pagine (da-a)377-378
RivistaNeurological Sciences
Volume39
Numero di pubblicazione2
DOI
Stato di pubblicazionePubblicato - 2018

Keywords

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

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