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

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

Abstract Background Pathogenic variants in MYH11 are associated with either heritable thoracic aortic aneurysm and dissection (HTAAD), patent ductus arteriosus (PDA) syndrome, or megacystis‐microcolon‐intestinal hypoperistalsis syndrome (MMIHS). Methods and Results We report a family referred for mo...

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Autores principales: Bertrand Chesneau, Aurélie Plancke, Guillaume Rolland, Bertrand Marcheix, Yves Dulac, Thomas Edouard, Julie Plaisancié, Marion Aubert‐Mucca, Sophie Julia, Maud Langeois, Thierry Lavabre‐Bertrand, Philippe Khau Van Kien
Formato: article
Lenguaje:EN
Publicado: Wiley 2021
Materias:
genotype–phenotype correlation
heritable aortic aneurysm syndrome
MYH11
patent ductus arteriosus
splicing
Genetics
QH426-470
Acceso en línea:https://doaj.org/article/7dfbe9dc055d409dac473c9c0a3607fc
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https://doaj.org/article/7dfbe9dc055d409dac473c9c0a3607fc

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