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Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up

Crossref DOI link: https://doi.org/10.1186/s13052-021-01152-y

Published Online: 2021-09-28

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Serra, Gregorio https://orcid.org/0000-0002-2918-9826
Antona, Vincenzo

Giuffré, Mario

Li Pomi, Federica

Lo Scalzo, Lucia

Piro, Ettore

Schierz, Ingrid Anne Mandy

Corsello, Giovanni
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Text and Data Mining valid from 2021-09-28

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Article History

Received: 13 August 2021

Accepted: 10 September 2021

First Online: 28 September 2021

Declarations

:

: Written informed consent was obtained from parents at admission of their newborn. The study was approved by the Mother and Child Department of the University of Palermo (Palermo, Italy). All procedures performed in this report were in accordance with the ethical standards of the institutional and national research committee, and with the 1964 Helsinki declaration and its later amendments, or comparable ethical standards.

: Not applicable.

: The authors declare that they have no competing interests.

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