Journal of Clinical and Investigative Dermatology

Case Report

A Neonatal Case of Bart Syndrome: First Reported Case from Yemen

Alshami MA1*, Alshami AM2, Alshami HM1, Lutf RM1 and Alnahari AA1

1Department of Dermatology, Faculty of Medicine and Medical Sciences, Sana’a University, Yemen.
2Department of Conservative Dentistry, Faculty of Dentistry, Sana’a University, Yemen
*Address for Correspondence:Mohammad Ali Alshami, Department of Dermatology, Faculty of Medicine and Medical Sciences, Sana’a University, Sana’a 1064, Yemen. E-mail Id: mohammadalshami62@gmail.com
Submission: 13 April, 2026 Accepted: 01 June, 2026 Published: 05 June, 2026
Copyright: © 2026 Alshami MA, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

A 10-day-old female infant presented with skin erosion and atrophy of the left leg, accompanied by an absence of most fingernails, evident since birth. In addition, she developed flaccid bullae and erosions at the sites of trauma. On the basis of these clinical findings, the patient was diagnosed with Bart syndrome, a rare type of genodermatosis characterized by the clinical triad of aplasia cutis congenita, epidermolysis bullosa, and nail abnormalities.