Publication:
Generalised Epidermolysis Bullosa with Severe Anaemia in an Adolescent: A Case Report

Date

2021

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Nepal Paediatric Society (JNPS)

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Abstract

Abstract: EBS is a rare genodermatosis usually inherited in an autosomal dominant fashion, although rare autosomal recessive cases have been reported. In severe generalised EBS, infants exhibit severe symptoms at the onset which tend to improve with time. We report an adolescent with severe generalised epidermolysis bullosa simplex (EBS), the most severe form of EBS, with severe iron deficiency anaemia.

Description

Shivam Jannawar Department of Paediatrics, Yashwantrao Chavan Memorial - Post Graduate Institute, Pune, India Deepali Ambike Department of Paediatrics, Yashwantrao Chavan Memorial - Post Graduate Institute, Pune, India Sabahat Ahmed Department of Paediatrics, Yashwantrao Chavan Memorial - Post Graduate Institute, Pune, India Rajesh K Kulkarni Department of Paediatrics, Yashwantrao Chavan Memorial - Post Graduate Institute, Pune, India Deepali Ambike YCM-PGI,Pune

Keywords

adolescent, Generalised Epidermolysis Bullosa, severe anaemia

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