Link: https://www.ncbi.nlm.nih.gov/pubmed/30656008

Clin Case Rep. 2018 Nov 11;7(1):54-57. doi: 10.1002/ccr3.1915. eCollection 2019 Jan.
Variable phenotypic expression of Apert syndrome in monozygotic twins.
Dap M1, Bach-Segura P2, Bertholdt C1, Menzies D3, Masutti JP3, Klein O4, Perdriolle-Galet E1, Lambert L5, Morel O1.
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Abstract
Apert syndrome in monozygotic twins can lead to different phenotypic expression of the disease in the two fetuses. Apert syndrome can be associated with congenital left diaphragmatic hernia and cleft palate.

KEYWORDS:
Apert syndrome; congenital diaphragmatic hernia; craniosynostosis; fetal autopsy; fetal ultrasound; monozygotic twins

PMID: 30656008 PMCID: PMC6333066 DOI: 10.1002/ccr3.1915
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