Ontology highlight
ABSTRACT:
SUBMITTER: Del Chierico F
PROVIDER: S-EPMC10275996 | biostudies-literature | 2023 Jun
REPOSITORIES: biostudies-literature
Del Chierico Federica F Marzano Valeria V Scanu Matteo M Reddel Sofia S Dentici Maria Lisa ML Capolino Rossella R Di Donato Maddalena M Spasari Iolanda I Fiscarelli Ersilia Vita EV Digilio Maria Cristina MC Abreu Maria Teresa MT Dallapiccola Bruno B Putignani Lorenza L
Scientific reports 20230616 1
Williams-Beuren syndrome (WBS) is a multisystem genetic disease caused by the deletion of a region of 1.5-1.8 Mb on chromosome 7q11.23. The elastin gene seems to account for several comorbidities and distinct clinical features such including cardiovascular disease, connective tissue abnormalities, growth retardation, and gastrointestinal (GI) symptoms. Increasing evidence points to alterations in gut microbiota composition as a primary or secondary cause of some GI or extra-intestinal characteri ...[more]