Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6

Alternative Names

  • LGMDR6
  • Muscular Dystrophy, Limb-Girdle, Type 2F
  • LGMD2F

Associated Genes

Sarcoglycan, Delta
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WHO-ICD-10 version:2010

Diseases of the nervous system

Diseases of myoneural junction and muscle

OMIM Number

601287

Mode of Inheritance

Autosomal recessive

Gene Map Locus

5q33.2-q33.3

Description

Autosomal recessive limb-girdle muscular dystrophy-6 (LGMDR6) is a very rare and severe neuromuscular disorder with onset in most patients in the first decade of life. Generalized muscle weakness affecting predominantly proximal and distal muscles of the limbs is progressive, and patients require walking aids or become wheelchair-bound. Some patients have cardiomyopathy or heart rhythm abnormalities, or require ventilatory support. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
601287.1Saudi ArabiaFemale Exercise intolerance; Easy fatigability;...NM_000337.6:c.339delHomozygousAutosomal, RecessiveMonies et al. 2017
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