A disease due to mutation of the lamin A/C gene. The laminopathies
include: Emery-Dreifuss muscular dystrophy type 2, fami lial 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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