Cargando…
Parental mosaicism in Marfan and Ehlers–Danlos syndromes and related disorders
Marfan syndrome (MFS) is a heritable connective tissue disorder (HCTD) caused by pathogenic variants in FBN1 that frequently occur de novo. Although individuals with somatogonadal mosaicisms have been reported with respect to MFS and other HCTD, the overall frequency of parental mosaicism in this pa...
Autores principales: | Chesneau, Bertrand, Plancke, Aurélie, Rolland, Guillaume, Chassaing, Nicolas, Coubes, Christine, Brischoux-Boucher, Elise, Edouard, Thomas, Dulac, Yves, Aubert-Mucca, Marion, Lavabre-Bertrand, Thierry, Plaisancié, Julie, Khau Van Kien, Philippe |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110803/ https://www.ncbi.nlm.nih.gov/pubmed/33414558 http://dx.doi.org/10.1038/s41431-020-00797-3 |
Ejemplares similares
-
A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus
por: Chesneau, Bertrand, et al.
Publicado: (2021) -
Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature
por: Chesneau, Bertrand, et al.
Publicado: (2020) -
Gastrointestinal Symptoms in Marfan Syndrome and Hypermobile Ehlers-Danlos Syndrome
por: Inayet, N., et al.
Publicado: (2018) -
Joint Hypermobility as a Potential Indicator of Marfan Syndrome and Ehlers-Danlos Syndrome
por: Zou, Henry, et al.
Publicado: (2022) -
Ehlers-Danlos syndrome
por: Taj, Farhana Tahseen, et al.
Publicado: (2014)