Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient

Luisa Marsili*, Eline Overwater, Nadine Hanna, Genevieve Baujat, Marieke J. H. Baars, Catherine Boileau, Dominique Bonneau, Anne Claire Brehin, Yline Capri, Ho Y. Cheung, Eelco Dulfer, Marion Gerard, Laurent Gouya, Yvonne Hilhorst-Hofstee, Arjan C. Houweling, Bertrand Isidor, Lauriane Le Gloan, Leonie A. Menke, Sylvie Odent, Fanny Morice-PicardClemence Vanlerberghe, Els Voorhoeve, J. Peter van Tintelen, Alessandra Maugeri, Pauline Arnaud

*Corresponding author voor dit werk

    OnderzoeksoutputAcademicpeer review

    14 Citaten (Scopus)
    55 Downloads (Pure)

    Samenvatting

    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.

    Originele taal-2English
    Pagina's (van-tot)723-730
    Aantal pagina's8
    TijdschriftClinical Genetics
    Volume97
    Nummer van het tijdschrift5
    DOI's
    StatusPublished - mei-2020

    Vingerafdruk

    Duik in de onderzoeksthema's van 'Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient'. Samen vormen ze een unieke vingerafdruk.

    Citeer dit