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Membranous aplasia cutis congenita

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Published: 17 November 2025
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Dear Editor,

Aplasia cutis congenita (ACC) is a rare congenital malformation characterized by the focal absence of skin visible at birth, most frequently involving the scalp, although any part of the body may be affected. The estimated incidence is approximately 1 to 3 per 10,000 live births. The pathogenesis is heterogeneous and yet not fully understood. [...]

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Citations

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8. Cammarata-Scalisi F, Diociaiuti A, de Guerrero B, et al. Membranous aplasia cutis congenita in trisomy 18. Ital J Pediatr 2020;46:120. DOI: https://doi.org/10.1186/s13052-020-00885-6
9. AlMatrafi FR, Al-Shammari AA, Al Nefily RM, et al. Case report: Aplasia cutis congenita of the scalp with bone defect and an exposed sagittal sinus in a trisomy 13 newborn. Front Pediatr 2023;11:1142950. DOI: https://doi.org/10.3389/fped.2023.1142950
10. Drolet B, Prendiville J, Golden J, et al. ‘Membranous aplasia cutis’ with hair collars. Congenital absence of skin or neuroectodermal defect? Arch Dermatol 1995;131:1427-31. DOI: https://doi.org/10.1001/archderm.1995.01690240091015

How to Cite



1.
Poddine G, Salvagno S, Bellinato F, Gisondi P, Girolomoni G. Membranous aplasia cutis congenita. Dermatol Reports [Internet]. 2025 Nov. 17 [cited 2026 Apr. 24];. Available from: https://journals.pagepress.net/dr/article/view/10544