Clin Case Rep Int | Volume 4, Issue 1 | Case Report | Open Access
Department of Physiotherapy, Teerthanker Mahaveer University, India
*Correspondance to: Aakanksha BajpaiFulltext PDF
Limb-Girdle Muscular Dystrophy-Type 2A (LGMD-2A) is an autosomal recessive disorder triggered by a mutation in the Calpain-3 gene (CAPN3) contributing to partial or complete protein deficiency. LGMD-2A is the most prevalent form of the disease in India, accounting for 47% of cases in the heterogeneous group. Here, we record a 22-year-old female with trouble walking due to proximal muscle weakness since one year and an elevated Creatine Phosphokinase (CPK) with abnormal muscle biopsy finding. The patient was granted an 8-week intervention and a prognosis was established.
LGMD-2A; Muscular dystrophy; Physiotherapy
Bajpai A. Physiotherapy in Calpainopathy (LGMD2A): A Case Report. Clin Case Rep Int. 2020; 4: 1158.