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Laminopathy

Laminopathy logo #10101) Muscular dystrophy
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Laminopathy

Laminopathy logo #21000 Laminopathies (lamino- + -opathy) are a group of rare genetic disorders caused by mutations in genes encoding proteins of the nuclear lamina. They are included in the more generic term nuclear envelopathies that was coined in 2000 for diseases associated with defects of the nuclear envelope. Since the first reports of laminopathies in the late 199...
Found on http://en.wikipedia.org/wiki/Laminopathy

Laminopathy

Laminopathy logo #20909Laminopathy: 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 syndrom...
Found on http://www.medterms.com/script/main/art.asp?articlekey=24022
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