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Aplasia cutis congenita in dizygotic twin infants
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Accepted Version
Date
2021-05-28
Authors
Bowe, S.
O'Connor, Cathal
Kenosi, M.
Murphy, L. A.
Journal Title
Journal ISSN
Volume Title
Publisher
John Wiley & Sons, Inc.
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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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Keywords
Aplasia cutis congenita
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
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© 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.