Epidermolysis bullosa
An autosomal recessive inherited skin disorder caused by mutations in the genes encoding keratins 5 and 14, collagen VII or laminin 5. It is characterized by skin fragility and the formation of blisters. The blisters may become large and ulcerated, resulting in skin infections and loss of body fluids.
Rarest case thanks for sharing sir.
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Thanks for remembering,Dr Pawar . There is no cure if it is congenital EB ,only preventing trauma helps . Here there is extensive denudation of the skin . So it is to be treated in lines of burns . Sepsis is treatable if vigorously managed...
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Dystrophic epidermolysis bullosa Yes genetic condition and a fragile epidermis exposed to minor injuries and exposed to infections and hence pt becomes vulnerable to any eventuality
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Recent Cases of Epidermolysis bullosa
Browse recently discussed Epidermolysis bullosa cases by specialistsTop Cases of Epidermolysis bullosa
Selected by editors, top cases are known for unique problem or best solutionTop Epidermolysis bullosa Doctors on Curofy
Top doctors who continously share their opinions on Epidermolysis bullosaPrivate Practise
Md

PHC Bichpuri and ESI Dispensary Chippitola Agra & SN Medical College Agra & Fatehgarh
Medical Officer Incharge
SN Medical College, Agra
DA

National Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics


Dr KUTE HOSPITAL
Dr KUTE HOSPITAL
Govt. Medical College Miraj
D M &S

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