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.
is a sample topic from the Taber's Medical Dictionary
To view other topics, please sign in or purchase a subscription.
Taber’s Cyclopedic Medical Dictionary Online + App from F.A. Davis and Unbound Medicine. Find 65,000 medical and nursing definitions. Download to iPhone, iPad, and Android. Complete Product Information.
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. F.A. Davis Company; 2017. https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy. Accessed February 25, 2020.
Bethlem myopathy. (2017). In Venes, D. (Ed.), Taber's Medical Dictionary (23rd edition). F.A. Davis Company. Retrieved February 25, 2020, 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 2020 February 25]. Available from: https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy.
TY - ELEC
T1 - Bethlem myopathy
ID - 729597
ED - Venes,Donald,
BT - Taber's Medical Dictionary
UR - https://www.tabers.com/tabersonline/view/Tabers-Dictionary/729597/all/Bethlem_myopathy
PB - F.A. Davis Company
ET - 23
DB - Taber's Online
DP - Unbound Medicine