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Aplasia cutis congenita in dizygotic twin infants
Murphy, L. A.
John Wiley & Sons, Inc.
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.
Aplasia cutis congenita
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
© 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.