Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis

Neurology. 2008 Jan 15;70(3):237-8. doi: 10.1212/01.wnl.0000278101.95510.09.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Bulbar Palsy, Progressive / genetics*
  • Bulbar Palsy, Progressive / physiopathology
  • Chromosomes, Human, Pair 22 / genetics
  • Cranial Nerves / physiopathology
  • DNA Mutational Analysis
  • Deglutition Disorders / genetics
  • Deglutition Disorders / physiopathology
  • Dysarthria / genetics
  • Dysarthria / physiopathology
  • Facial Paralysis / genetics*
  • Facial Paralysis / physiopathology
  • Humans
  • Infant, Newborn
  • Male
  • Mobius Syndrome / complications
  • Mobius Syndrome / genetics
  • Muscle Hypotonia / complications
  • Muscle Hypotonia / genetics
  • Muscle Hypotonia / physiopathology
  • Muscle, Skeletal / innervation
  • Muscle, Skeletal / physiopathology
  • Mutation
  • Myasthenia Gravis / complications*
  • Myasthenia Gravis / genetics*
  • Myasthenia Gravis / physiopathology
  • Neuromuscular Junction / genetics
  • Neuromuscular Junction / physiopathology
  • Palatal Muscles / innervation
  • Palatal Muscles / physiopathology
  • Pharynx / innervation
  • Pharynx / physiopathology