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CASE REPORT
Year : 2020  |  Volume : 21  |  Issue : 4  |  Page : 316-318

The use of immunofluorescence antigen mapping in the diagnosis of junctional epidermolysis bullosa in a 15-year-old female


Department of Dermatology, Civil Hospital, B.J. Medical College, Ahmedabad, Gujarat, India

Correspondence Address:
Dr. Deval Mistry
C/11 Murdhanya Apartment, Opp. Torrent Zonal Office, B/H Bhoomi Party Plot, Naranpura, Ahmedabad - 380 013, Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijpd.IJPD_90_20

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Epidermolysis bullosa (EB) comprises a group of genetically determined skin fragility disorders, characterized by blistering of the skin and mucosae following mechanical trauma, which includes four major forms (EB simplex, junctional EB [JEB], dystrophic EB, and Kindler syndrome) with various distinctive clinical phenotypes. We report a rare case of a 15-year-old female diagnosed as JEB (generalized intermediate), with the help of immunofluorescence antigen mapping.


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