A rare, autosomal dominant form of limb-girdle muscular dystrophy that becomes clinically obvious in early childhood. It is usually slowly progressive, gradually resulting in weakness that may limit the ability to walk independently. Muscle contractures, e.g., of the hands, ankles, and elbows, are characteristic.
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Venes, Donald, editor. "Bethlem Myopathy." Taber's Medical Dictionary, 23rd ed., F.A. Davis Company, 2017. Taber's Online, www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy.
Bethlem myopathy. In: Venes DD, ed. Taber's Medical Dictionary. F.A. Davis Company; 2017. https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy. Accessed January 28, 2021.
Bethlem myopathy. (2017). In Venes, D. (Ed.), Taber's Medical Dictionary (23rd edition). F.A. Davis Company. Retrieved January 28, 2021, from https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy
Bethlem Myopathy [Internet]. In: Venes DD, editors. Taber's Medical Dictionary. F.A. Davis Company; 2017. [cited 2021 January 28]. Available from: https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy.
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