Aplasia cutis congenita in dizygotic twin infants

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Aplasia cutis congenita in dizygotic twin infants

Bowe, S.; O'Connor, Cathal; Kenosi, M.; Murphy, L. A.
Date: 2021-05-28
Copyright: © 2021, John Wiley & Sons, Inc. This is the accepted version of the following publication: Bowe, S., O’Connor, C., Kenosi, M. and Murphy, L. (2021) 'Aplasia cutis congenita in dizygotic twin infants', Clinical and Experimental Dermatology, doi: 10.1111/ced.14763, which has been published in final form at: https://doi.org/10.1111/ced.14763. This item may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Full text restriction information: Access to this article is restricted until 12 months after publication by request of the publisher.
Restriction lift date: 2022-05-28
Citation: Bowe, S., O’Connor, C., Kenosi, M. and Murphy, L. (2021) 'Aplasia cutis congenita in dizygotic twin infants', Clinical and Experimental Dermatology. doi: 10.1111/ced.14763
Published Version: 10.1111/ced.14763

Abstract:

Aplasia cutis congenita (ACC) is a rare heterogenous group of disorders characterized by the absence of a portion of skin in a localized or widespread area at birth. 1 ACC is often sporadic but familial cases have been reported. 1,2 We report a case of a dichorionic diamniotic (DCDA) twin pregnancy in which both the male and female twins had matching areas of aplasia cutis on their scalps.

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