Variable phenotypic expression of Apert syndrome in monozygotic twins.

Autor: Dap M; Department of Gynecology and Obstetrics CHRU de Nancy Nancy France., Bach-Segura P; Department of Perinatal Radiology and Imaging CHRU de Nancy Nancy France., Bertholdt C; Department of Gynecology and Obstetrics CHRU de Nancy Nancy France., Menzies D; Department of Fetopathology CHRU de Nancy Nancy France., Masutti JP; Department of Fetopathology CHRU de Nancy Nancy France., Klein O; Department of Pediatric Neurosurgery CHRU de Nancy Nancy France., Perdriolle-Galet E; Department of Gynecology and Obstetrics CHRU de Nancy Nancy France., Lambert L; Department of Clinical Genetic CHRU de Nancy Nancy France., Morel O; Department of Gynecology and Obstetrics CHRU de Nancy Nancy France.
Jazyk: angličtina
Zdroj: Clinical case reports [Clin Case Rep] 2018 Nov 11; Vol. 7 (1), pp. 54-57. Date of Electronic Publication: 2018 Nov 11 (Print Publication: 2019).
DOI: 10.1002/ccr3.1915
Abstrakt: 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.
Databáze: MEDLINE
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