A New Variant in the MYH11 Gene in a Familial Case of Thoracic Aortic Aneurysm.

Détails

ID Serval
serval:BIB_3CCA95B6B94E
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
A New Variant in the MYH11 Gene in a Familial Case of Thoracic Aortic Aneurysm.
Périodique
The Annals of thoracic surgery
Auteur⸱e⸱s
Pucci L., Pointet A., Good J.M., Davoine E., Cina V., Zanchi F., Deglise S., Duchosal L.M., Kirsch M.
ISSN
1552-6259 (Electronic)
ISSN-L
0003-4975
Statut éditorial
Publié
Date de publication
04/2020
Peer-reviewed
Oui
Volume
109
Numéro
4
Pages
e279-e281
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Résumé
MYH11 (myosin heavy chain 11) gene is involved in vascular contractility and several autosomal dominant mutations have been linked to thoracic aortic aneurysms. Three male members of the same family were found to carry a heterozygous missense variant in the MYH11 gene and all 3 individuals presented a thoracic aortic aneurysm/dilation. We identified a rare missense variant in the MYH11 gene predicted to be damaging and affecting a conserved amino acid in the myosin tail of the protein. This variant appears to be responsible for our familial case of thoracic aortic aneurysms, as the clinical expression reunited all features of genetic aneurysms.
Mots-clé
Aged, Aortic Aneurysm, Thoracic/genetics, Humans, Male, Mutation, Missense, Myosin Heavy Chains/genetics
Pubmed
Web of science
Création de la notice
13/09/2019 18:57
Dernière modification de la notice
21/07/2022 6:36
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