Bethlem myopathy
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.
Citation
Venes, Donald, editor. "Bethlem Myopathy." Taber's Medical Dictionary, 24th ed., F.A. Davis Company, 2021. Nursing Central, nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/729597/all/Bethlem_myopathy.
Bethlem myopathy. In: Venes DD, ed. Taber's Medical Dictionary. F.A. Davis Company; 2021. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/729597/all/Bethlem_myopathy. Accessed November 8, 2024.
Bethlem myopathy. (2021). In Venes, D. (Ed.), Taber's Medical Dictionary (24th ed.). F.A. Davis Company. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/729597/all/Bethlem_myopathy
Bethlem Myopathy [Internet]. In: Venes DD, editors. Taber's Medical Dictionary. F.A. Davis Company; 2021. [cited 2024 November 08]. Available from: https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/729597/all/Bethlem_myopathy.
* Article titles in AMA citation format should be in sentence-case
TY - ELEC
T1 - Bethlem myopathy
ID - 729597
ED - Venes,Donald,
BT - Taber's Medical Dictionary
UR - https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/729597/all/Bethlem_myopathy
PB - F.A. Davis Company
ET - 24
DB - Nursing Central
DP - Unbound Medicine
ER -