Epidermolysis bullosa dystrophic
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.
Disease Alternative Name
Top Epidermolysis bullosa dystrophic Doctors on Curofy
Top doctors who continously share their opinions on Epidermolysis bullosa dystrophic
Gandhi Medical College.
M.B.B.S.
Sepuri Endocrine & Diabetes Centre
Consultant Endocrinologist & Diabetologist
Royal College of Physicians, United Kingdom
Masters in Clinical Endocrinology & Diabetology
SHANTI MEMORIAL HOSPITAL
CONSULTANT PEDIATRICIAN MD,DNB
IPGME&R
MD
JayaVeda Skin and Laser Clinic
Consultant Dermatologist and Cosmetologist.
Rajah Muthiah Medical College and Hospital.
MBBS., D.D.V.L.,
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