Case report of Bart syndrome due to aplasia cutis and junctional epidermolysis bullosa caused by a collagen XVII mutation (EADV 2026) - Aug 6, 2026 - Abstract #PCC-836; CC-721; Pres time: Sep 30, 2026; Location: ePoster Area; "After three months of follow-up, the patient showed clinical improvement, with a decrease in the number of wounds and a faster healing rate, without any adverse effects reported. Conclusion This case highlights the importance of integrated clinical and genetic evaluation for accurate diagnosis and suggests that incorporating emerging therapies into individualized approaches can improve functional outcomes and quality of life in severe congenital genodermatoses."
Case report • Clinical • Mood Disorders • Obstetrics • COL17A1
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Daniel Robles Murcia; Diego Gallego García; Jose Molina Espinosa; Pedro Ezomo Gervilla; Israel Pérez López; Ricardo Ruiz Villaverde
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