Open AccessA rare case of late‐onset limb‐girdle muscular dystrophy: Calpainopathy
Author(s) -
Painkra Bhawana,
Mallick Richa,
Das Sumanta,
Kumar Pramod,
Chatterjee Prasun
Publication year - 2022
Publication title -
aging medicine
Language(s) - English
Resource type - Journals
ISSN - 2475-0360
DOI - 10.1002/agm2.12219
Subject(s) - limb girdle muscular dystrophy , medicine , muscular dystrophy , shoulder girdle , anatomy , biology , mutation , genetics , gene
Limb‐girdle muscular dystrophy is a genetic disorder usually presenting in younger age patients. This case report presents a case of late‐onset limb‐girdle muscular dystrophy type R1 (Calpainopathy) in a 65 year old patient.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom