Cargando…
Variable phenotypic expression of Apert syndrome in monozygotic twins
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.
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333066/ https://www.ncbi.nlm.nih.gov/pubmed/30656008 http://dx.doi.org/10.1002/ccr3.1915 |
_version_ | 1783387495467057152 |
---|---|
author | Dap, Matthieu Bach‐Segura, Pascale Bertholdt, Charline Menzies, Didier Masutti, Jean‐Pierre Klein, Olivier Perdriolle‐Galet, Estelle Lambert, Laetitia Morel, Olivier |
author_facet | Dap, Matthieu Bach‐Segura, Pascale Bertholdt, Charline Menzies, Didier Masutti, Jean‐Pierre Klein, Olivier Perdriolle‐Galet, Estelle Lambert, Laetitia Morel, Olivier |
author_sort | Dap, Matthieu |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6333066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63330662019-01-17 Variable phenotypic expression of Apert syndrome in monozygotic twins Dap, Matthieu Bach‐Segura, Pascale Bertholdt, Charline Menzies, Didier Masutti, Jean‐Pierre Klein, Olivier Perdriolle‐Galet, Estelle Lambert, Laetitia Morel, Olivier Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2018-11-11 /pmc/articles/PMC6333066/ /pubmed/30656008 http://dx.doi.org/10.1002/ccr3.1915 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Dap, Matthieu Bach‐Segura, Pascale Bertholdt, Charline Menzies, Didier Masutti, Jean‐Pierre Klein, Olivier Perdriolle‐Galet, Estelle Lambert, Laetitia Morel, Olivier Variable phenotypic expression of Apert syndrome in monozygotic twins |
title | Variable phenotypic expression of Apert syndrome in monozygotic twins |
title_full | Variable phenotypic expression of Apert syndrome in monozygotic twins |
title_fullStr | Variable phenotypic expression of Apert syndrome in monozygotic twins |
title_full_unstemmed | Variable phenotypic expression of Apert syndrome in monozygotic twins |
title_short | Variable phenotypic expression of Apert syndrome in monozygotic twins |
title_sort | variable phenotypic expression of apert syndrome in monozygotic twins |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333066/ https://www.ncbi.nlm.nih.gov/pubmed/30656008 http://dx.doi.org/10.1002/ccr3.1915 |
work_keys_str_mv | AT dapmatthieu variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT bachsegurapascale variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT bertholdtcharline variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT menziesdidier variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT masuttijeanpierre variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT kleinolivier variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT perdriollegaletestelle variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT lambertlaetitia variablephenotypicexpressionofapertsyndromeinmonozygotictwins AT morelolivier variablephenotypicexpressionofapertsyndromeinmonozygotictwins |