Orphanet: Hereditary continuous muscle fiber activity
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Hereditary continuous muscle fiber activity

Disease definition

Hereditary continuous muscle fiber activity is a rare, non-dystrophic myopathy characterized by generalized myokymia and increased muscle tone associated with delayed motor milestones, leg stiffness, spastic gait, hyperreflexia and Babinski sign. Symptoms may be worsened by febrile illness or anesthesia.

ORPHA:972

Classification level: Disorder
  • Synonym(s): -
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Infancy, Childhood
  • ICD-10: G71.1
  • OMIM: 160120
  • UMLS: C1834559
  • MeSH: -
  • GARD: -
  • MedDRA: -
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