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LGMDLimb-Girdle Muscular Dystrophy
LGMDLobula Giant Movement Detector (computational biology)
LGMDLocal Government Monitoring Database (Tanzania)
References in periodicals archive ?
Korkusuz et al., "Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy," American Journal of Human Genetics, vol.
"These exciting results demonstrate the feasibility of gene therapy to treat limb-girdle muscular dystrophy," said Jane Larkindale, portfolio director with Muscular Dystrophy Association Venture Philanthropy, a program that moves basic research into treatment development.
Identification of lamin A/C (LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy I B.
Anaesthetic management of a patient with limb-girdle muscular dystrophy for laparoscopic cholecystectomy.
To the Editor: Limb-girdle muscular dystrophy type 2A (LGMD2A) is a group of progressive muscle diseases with autosomal recessive inheritance.
Age of Inheritance/gender Muscles first onset affected affected 2-16 years X-linked/males Pelvis, upper arms, upper legs Age of Progression onset 2-16 years Slow Most often, the onset of limb-girdle muscular dystrophy is in adolescence or early adulthood.
Further, Sarepta will be presenting 60-day biopsy data from Cohort 1 in early-2019 from the ongoing phase 1/2a MYO-101 beta-sarcoglycan gene therapy program in limb-girdle muscular dystrophy type 2E, adds Rama.
Similar fatty infiltration distribution patterns, predominantly involving the posterior compartment of the thigh, were also reported in mitochondrial diseases [20] and limb-girdle muscular dystrophy (LGMD).[21],[22],[23] LGMD-2A showed more severe fatty infiltration in the adductor major, adductor longus, and semimembranosus, with sparing of the anterior compartment of the thigh, at the early stage of disease.[21],[22] Similarly, LGMD-2B presented with large variations in fatty infiltration between the anterior and posterior compartments of the thigh.[23] However, the edema distribution patterns between LGMD-2B and IMNM or MADD were different.