MEDICAL DICTIONARY
Laminopathy: A disease due to mutation of the lamin A/C gene . The laminopathies include: Emery-Dreifuss muscular dystrophy type 2, familial partial lipodystrophy , limb girdle muscular dystrophy type 1B, dilated cardiomyopathy , familial partial lipodystrophy , Charcot-Marie-Tooth disorder type 2B1, mandibuloacral dysplasia , childhood progeria syndrome (Hutchinson-Gilford syndrome ) and a subset of Werner syndrome . See also: Lamin A/C .
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