Aplasia cutis congentia is a rare heterogenous group of disorder with focal absence of the skin and its underlying structures with a varying depth ranging from the epidermis to even subcutis, bone or even dura. Depending upon the onset & duration of insult during pregnancy it can present as a open wound that needs prompt treatment or a healed scar. This has a rare occurrence with upto 500 cases reported in literature. In this article, we report a rare case series of aplasia cutis congenita and review of literature.
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How to Cite This Article
Vancouver
S S, Narayanan N, Thomas J. A rare case series of congenital absence of skin – Aplasia cutis congenita [Internet]. IP Indian J Clin Exp Dermatol. 2025 [cited 2025 Nov 08];11(3):426-429. Available from: https://doi.org/10.18231/j.ijced.72572.1758884168
APA
S, S., Narayanan, N., Thomas, J. (2025). A rare case series of congenital absence of skin – Aplasia cutis congenita. IP Indian J Clin Exp Dermatol, 11(3), 426-429. https://doi.org/10.18231/j.ijced.72572.1758884168
MLA
S, Soundarya, Narayanan, Nikita, Thomas, Jayakar. "A rare case series of congenital absence of skin – Aplasia cutis congenita." IP Indian J Clin Exp Dermatol, vol. 11, no. 3, 2025, pp. 426-429. https://doi.org/10.18231/j.ijced.72572.1758884168
Chicago
S, S., Narayanan, N., Thomas, J.. "A rare case series of congenital absence of skin – Aplasia cutis congenita." IP Indian J Clin Exp Dermatol 11, no. 3 (2025): 426-429. https://doi.org/10.18231/j.ijced.72572.1758884168