LMNA and Hutchinson-Gilford progeria syndrome: Over the past few decades, nearly 500 mutations have been identified in LMNA which cause a plethora of diseases such as Emery-Dreifuss Muscular Dystrophy (EDMD), dilated cardiomyopathy (DCM), Hutchinson-Gilford Progeria Syndrome (HGPS), Lipodystrophy syndrome, peripheral neuropathy, etc., which are collectively named as ‘laminopathies’[32].