ARTICLE TYPE : CASE REPORT
Published on : 22 Jan 2026, Volume - 2
Journal Title : WebLog Journal of Dermatology | WebLog J Dermatol
Source URL:
https://weblogoa.com/articles/wjd.2026.a2201
Permanent Identifier (DOI) :
https://doi.org/10.5281/zenodo.18447237
Neonatal Epidermolysis Bullosa Simplex: Early Diagnostic Clarification and Multidisciplinary Management in a Term Female Infant
2Formerly Head, Department of Surgery at Tata Memorial Hospital, Mumbai, India
3J. Watumull Global Hospital & Research Centre, Delwara Road, Mount Abu, Rajasthan 307501, India Affiliated to Medical Faculty of God Fatherly Spiritual University, Mount Abu, Rajasthan, India
Abstract
Epidermolysis bullosa (EB) comprises a heterogeneous group of inherited mechanobullous disorders characterised by skin fragility and blister formation following minimal trauma [1–3]. We report a female neonate presenting with localised blistering on the dorsum of the right foot and over the heel, ultimately diagnosed with epidermolysis bullosa simplex (EBS). Early multidisciplinary involvement, meticulous wound care, and parental counselling were central to management [8, 9]. This case highlights the importance of early recognition, genetic confirmation, and anticipatory guidance for families [1, 6, 7].
Keywords: Epidermolysis Bullosa; Epidermolysis Bullosa Simplex; Neonatal Blistering Disorders; Skin Fragility; KRT5; KRT14; Immunofluorescence Antigen Mapping; Congenital Bullous Dermatoses; Neonatal Dermatology; Genetic Skin Disease; Wound Care in Neonates; Supportive Neonatal Care; Rare Genetic Disorders
Citation
Govani DR, Mehta AR, Midha PK, Govani ND, Panchasara NG, Patel RR, et al. Neonatal Epidermolysis Bullosa Simplex: Early Diagnostic Clarification and Multidisciplinary Management in a Term Female Infant. WebLog J Dermatol. wjd.2026.a2201. https://doi.org/10.5281/zenodo.18447237