Myasthenic Syndrome, Congenital, 10

Alternative Names

  • CMS10
  • Myasthenia, Limb-Girdle, Familial
  • LGM
  • Congenital Myasthenic Syndrome Type Ib
  • CMS1B
  • CMS Ib
  • Myasthenic Myopathy
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WHO-ICD-10 version:2010

Diseases of the nervous system

Diseases of myoneural junction and muscle

OMIM Number

254300

Mode of Inheritance

Autosomal recessive

Gene Map Locus

4p16.3

Description

Congenital myasthenic syndromes (CMS) are a group of inherited disorders affecting the neuromuscular junction (NMJ). Patients present clinically with onset of variable muscle weakness between infancy and adulthood. These disorders have been classified according to the location of the defect: presynaptic, synaptic, and postsynaptic. CMS10 is an autosomal recessive CMS resulting from a postsynaptic defect affecting endplate maintenance of the NMJ. Patients present with limb-girdle weakness in the first decade. Treatment with ephedrine or salbutamol may be beneficial; cholinesterase inhibitors should be avoided. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
254300.1United Arab EmiratesUnknown Generalized hypotonia; Proximal muscle ...NM_173660.5:c.1124_1127dup, NM_173660.5:c.1457dupHeterozygousAutosomal, RecessiveAl-Shamsi et al. 2016
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