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

Authors

  • 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

DOI:

https://doi.org/10.3126/jnps.v41i2.35059

Keywords:

adolescent, Generalised Epidermolysis Bullosa, severe anaemia

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

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Published

2021-11-03

How to Cite

Jannawar, S., Ambike, D., Ahmed, S., Kulkarni, R. K., & Ambike, D. (2021). Generalised Epidermolysis Bullosa with Severe Anaemia in an Adolescent: A Case Report. Journal of Nepal Paediatric Society, 41(2), 290–293. https://doi.org/10.3126/jnps.v41i2.35059

Issue

Vol. 41 No. 2 (2021)

Section

Case Reports

License

Copyright (c) 2021 Shivam Jannawar, Deepali Ambike, Sabahat Ahmed, Rajesh K Kulkarni, Deepali Ambike

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