Phenotypic spectrum of tgfb3 disease-causing ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
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Titre :
Phenotypic spectrum of tgfb3 disease-causing variants in a dutch-french cohort and first report of a homozygous patient
Auteur(s) :
Marsili, Luisa [Auteur]
Overwater, Eline [Auteur]
Hanna, Nadine [Auteur]
Baujat, Genevieve [Auteur]
Baars, Marieke J. H. [Auteur]
Boileau, Catherine [Auteur]
Bonneau, Dominique [Auteur]
Brehin, Anne-Claire [Auteur]
Capri, Yline [Auteur]
Cheung, Ho Y. [Auteur]
Dulfer, Eelco [Auteur]
Gerard, Marion [Auteur]
Gouya, Laurent [Auteur]
Hilhorst-Hofstee, Yvonne [Auteur]
Houweling, Arjan C. [Auteur]
Isidor, Bertrand [Auteur]
Le Gloan, Lauriane [Auteur]
Menke, Leonie A. [Auteur]
Odent, Sylvie [Auteur]
Morice-Picard, Fanny [Auteur]
Vanlerberghe, Clemence [Auteur]
Voorhoeve, Els [Auteur]
Van Tintelen, J. Peter [Auteur]
Maugeri, Alessandra [Auteur]
Arnaud, Pauline [Auteur]
Overwater, Eline [Auteur]
Hanna, Nadine [Auteur]
Baujat, Genevieve [Auteur]
Baars, Marieke J. H. [Auteur]
Boileau, Catherine [Auteur]
Bonneau, Dominique [Auteur]
Brehin, Anne-Claire [Auteur]
Capri, Yline [Auteur]
Cheung, Ho Y. [Auteur]
Dulfer, Eelco [Auteur]
Gerard, Marion [Auteur]
Gouya, Laurent [Auteur]
Hilhorst-Hofstee, Yvonne [Auteur]
Houweling, Arjan C. [Auteur]
Isidor, Bertrand [Auteur]
Le Gloan, Lauriane [Auteur]
Menke, Leonie A. [Auteur]
Odent, Sylvie [Auteur]
Morice-Picard, Fanny [Auteur]
Vanlerberghe, Clemence [Auteur]
Voorhoeve, Els [Auteur]
Van Tintelen, J. Peter [Auteur]
Maugeri, Alessandra [Auteur]
Arnaud, Pauline [Auteur]
Titre de la revue :
Clinical Genetics
Nom court de la revue :
Clin. Genet.
Date de publication :
2020-01-02
ISSN :
1399-0004
Mot(s)-clé(s) :
aortic dissection
connective tissue disorder
Loeys-Dietz syndrome
aortic dilatation
transforming growth factor beta 3
TGFB3
connective tissue disorder
Loeys-Dietz syndrome
aortic dilatation
transforming growth factor beta 3
TGFB3
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Disease-causing variants in TGFB3 cause an autosomal dominant connective tissue disorder which is hard to phenotypically delineate because of the small number of identified cases. The purpose of this retrospective ...
Lire la suite >Disease-causing variants in TGFB3 cause an autosomal dominant connective tissue disorder which is hard to phenotypically delineate because of the small number of identified cases. The purpose of this retrospective cross-sectional multicenter study is to elucidate the genotype and phenotype in an international cohort of TGFB3 patients. Eleven (eight novel) TGFB3 disease-causing variants were identified in 32 patients (17 families). Aortic root dilatation and mitral valve disease represented the most common cardiovascular findings, reported in 29% and 32% of patients, respectively. Dissection involving distal aortic segments occurred in two patients at age 50 and 52 years. A high frequency of systemic features (65% high-arched palate, 63% arachnodactyly, 57% pectus deformity, 52% joint hypermobility) was observed. In familial cases, incomplete penetrance and variable clinical expressivity were noted. Our cohort included the first described homozygous patient, who presented with a more severe phenotype compared to her heterozygous relatives. In conclusion, TGFB3 variants were associated with a high percentage of systemic features and aortic disease (dilatation/dissection) in 35% of patients. No deaths occurred from cardiovascular events or pregnancy-related complications. Nevertheless, homozygosity may be driving a more severe phenotype.Lire moins >
Lire la suite >Disease-causing variants in TGFB3 cause an autosomal dominant connective tissue disorder which is hard to phenotypically delineate because of the small number of identified cases. The purpose of this retrospective cross-sectional multicenter study is to elucidate the genotype and phenotype in an international cohort of TGFB3 patients. Eleven (eight novel) TGFB3 disease-causing variants were identified in 32 patients (17 families). Aortic root dilatation and mitral valve disease represented the most common cardiovascular findings, reported in 29% and 32% of patients, respectively. Dissection involving distal aortic segments occurred in two patients at age 50 and 52 years. A high frequency of systemic features (65% high-arched palate, 63% arachnodactyly, 57% pectus deformity, 52% joint hypermobility) was observed. In familial cases, incomplete penetrance and variable clinical expressivity were noted. Our cohort included the first described homozygous patient, who presented with a more severe phenotype compared to her heterozygous relatives. In conclusion, TGFB3 variants were associated with a high percentage of systemic features and aortic disease (dilatation/dissection) in 35% of patients. No deaths occurred from cardiovascular events or pregnancy-related complications. Nevertheless, homozygosity may be driving a more severe phenotype.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
Collections :
Date de dépôt :
2021-09-02T07:02:14Z