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CASE REPORT
Year : 2016  |  Volume : 17  |  Issue : 1  |  Page : 29-31

Peeling skin in newborn with abdominal distension


1 Department of Paediatric Surgery, Medical College and Hospital, Kolkata, West Bengal, India
2 Department of Dermatology, Medical College and Hospital, Kolkata, West Bengal, India

Correspondence Address:
Niharika Ranjan Lal
32, Prince Rahimuddin Lane, Tollygunge, Kolkata - 33, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2319-7250.173145

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Epidermolysis bullosa (EB) is a rare hereditary disorder characterized by the formation of blisters following minor trauma. It has been traditionally categorized by the level of basement membrane zone separation into EB simplex, junctional EB, and dystrophic EB. Recently, hemidesmosomal EB has been proposed as a fourth category, which includes EB with muscular dystrophy and EB with pyloric atresia (PA). Among the subtypes, EB with PA is a rare form of EB. We report here a neonate with EB-PA, who, unfortunately, died on the 2nd day of life.


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