Clinical-Molecular approach in autosomal recessive limb girdle muscular dystrophy in INR, México


LGMD diagnosis in Mexico is difficult because of the lack resources to study them. Their differentiation is important to offer genetic counseling and appropriate treatment. To establish the correlation between genotype and phenotype in LGMD II patients at The Institute National of Rehabilitation. Descriptive, cross-sectional in patients with diagnosis of LGMD. Files were reviewed from 1995 to 2016 and statistic descriptive was done. 247 files were reviewed, 97 with probably diagnosis of LGMD, 52 (53.6%) men and 45 (46.39%) women.


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