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  • Title: Dysferlinopathy: spectrum of pathological changes in skeletal muscle tissue.
    Author: Gayathri N, Alefia R, Nalini A, Yasha TC, Anita M, Santosh V, Shankar SK.
    Journal: Indian J Pathol Microbiol; 2011; 54(2):350-4. PubMed ID: 21623088.
    Abstract:
    BACKGROUND: Dysferlinopathy is an autosomal recessive-limb girdle muscular dystrophy (AR-LGMD) caused due to the defect in gene encoding dysferlin, a sarcolemmal protein. Awareness of the variants and their relative frequency is essential for accurate diagnosis. AIM: To study the spectrum of morphologic changes in immunohistochemically proven cases of dysferlinopathies, to correlate the findings with clinical phenotype and durations of illness and determine the frequency. MATERIALS AND METHODS: Dysferlinopathies seen over a period of 2 years at a tertiary neurological center were analyzed. RESULTS: Clinically, majority had Miyoshi phenotype (46.6%) with distal involvement and LGMD phenotype (40%) with proximal muscle involvement. In addition, a proximo-distal and tibial muscle phenotype was encountered. Morphologically, rimmed vacuoles were noted in the Miyoshi phenotype. The presence of ragged red fibers, lobulated fibers and inflammation had no preference to a particular phenotype. Significant atrophy and lobulated fibers were noted in patients with longer duration of illness. CONCLUSIONS: Dysferlinopathy was the second most common identifiable cause (21%) of LGMD next to sarcoglycanopathies (27%).
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