Epidermolysis bullosae

Abstract

normal. A clinical diagnosis of EBS was made. Screening test for congenital syphilis was negative. Skin biopsy (using electron microscopy) from the edge of affected lesion confirmed it to be EBS. There was no similar family history in the past. Supportive management in the form of skin dressing, puncture of blisters, local antiseptic application and careful handling was done. Complete breast feeds was started and genetic counselling was done. The baby is progressing well on regular OPD follow-up. DISCUSSIONEpidermolysis bullosae is a genetic disorder caused by a mutation in the keratin gene. The identified genes include those that encode keratins 5 and 14 in EBS (autosomal recessive), collagen VII in DEB (autosomal recessive and dominant types), and

Management of a Femur Shaft Fracture With Nancy Nail in the Setting of Dystrophic Epidermolysis Bullosa: A Case Report

“…Children who suffer from epidermolysis bullosa are often referred to as “Butterfly children” as their skin is as vulnerable as the wings of a butterfly [ 1 ]. Epidermolysis bullosa is an entity of heterogenous bullous dermatoses including cutaneous fragility leading to bullous formation after exposure to trauma despite how minimal it is.…”