Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study.
Carolina PutottoFederica PulvirentiFlaminia PugnaloniIna IsufiMarta UnoltSilvia AnaclerioViviana CaputoLaura BernardiniElisa MessinaCorrado MorettiLuigi TaraniBruno MarinoPaolo VersacciPublished in: Genes (2022)
Isolated ARD is common in 22q11.2DS. Although some clinical risk factors have been identified, pathogenetic mechanisms and risk of complications are undefined. Regular cardiac evaluations should be part of the 22q11.2DS follow-up, and also in non-CHDs patients, to improve long-term outcome.