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Epidermolysis bullosa simplex

Epidermolysis bullosa simplex (EBS), is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.:598see also Template:Congenital malformations and deformations of skin appendages, Template:Phakomatoses, Template:Pigmentation disorders, Template:DNA replication and repair-deficiency disorderAnkyrin: Long QT syndrome 4 Epidermolysis bullosa simplex (EBS), is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.:598 Blister formation of EBS occurs at the dermoepidermal junction. Sometimes EBS is called epidermolytic.

[ "Dominance (genetics)", "Epidermolysis bullosa", "Mutation", "Keratin", "Gene", "EB simplex", "Plectin Gene", "Mottled pigmentation", "Dowling-Meara epidermolysis bullosa", "Weber-Cockayne epidermolysis bullosa" ]
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