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 D, ed. Taber's Medical Dictionary. 23rd ed. F.A. Davis Company; 2017. https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy. Accessed November 21, 2019.
Bethlem myopathy. (2017). In Venes, D. (Ed.), Taber's Medical Dictionary. Available from https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy
Bethlem Myopathy [Internet]. In: Venes D, editors. Taber's Medical Dictionary. F.A. Davis Company; 2017. [cited 2019 November 21]. Available from: https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy.
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T1 - Bethlem myopathy
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PB - F.A. Davis Company
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