Epidermolysis bullosa pruriginosa: A case report of two first cousins

Genodermatoses are quite frequent in developing countries where consanguinity is common but usually under reported and undiagnosed. Main reason being lack of accessibility to tertiary health care facilities for people rural areas as evident case below. Genetic counselling pre natal testing utmost importance affected families. Epidermolysis bullosa pruriginosa (EBP) a rare less recognized variant dystrophic epidermolysis bullosa. Reporting the two first cousins who presented with intensely pruritic skin lesions since infancy along history siblings problems. EBP provided unifying diagnosis.
 doi: https://doi.org/10.12669/pjms.39.5.6764
 How cite this: Zahoor M. pruriginosa: A report cousins. Pak J Med Sci. 2023;39(5):---------. This an Open Access article distributed terms Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, reproduction any medium, original work properly cited.