Previous studies have reported that mutations in the LMNA gene are associated with a wide range of human genetic disorders, including dilated cardiomyopathy with conduction-system disease (DCM-CD) [8], limb girdle muscular dystrophy with atrioventricular conduction disturbance (LGMD1B) [9], Dunnigan-type of familial partial lipodystrophy [10], autosomal recessive Charcot-Marie-Tooth disease type 2 [11], mandibuloacral dysplasia[12], Hutchinson-Gilford progeria syndrome (HGPS) [13, 14], atypical Werner’s syndrome [15], and restrictive dermopathy [16]. Here, LMNA is linked to Autosomal dominant limb-girdle muscular dystrophy type 1B.