Back to Authors

MuiƱo-Mosquera, Laura

0000-0002-3094-7807

Mayo Clinic

Center for Medical Genetics (B.C., L.M.-M.), Ghent University Hospital, Belgium.

Citations 2

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy

Circulation: Genomic and Precision Medicine | April 21, 2025 | Volume: 18 | Issue: 3 | Pages: No page available

10.1161/circgen.124.004976 | PMID 40255155

Bicuspid Aortic Valve Disease with Early-Onset Complications: Characteristics and Aortic Outcomes

Hearts | June 21, 2024 | Volume: 5 | Issue: 3 | Pages: 253-258

10.3390/hearts5030018

Bicuspid aortic valve (BAV) is the most common congenital heart malformation in adults, but it can also cause childhood-onset complications. The presentation and clinical course of young adults who present due to BAV complications are relatively uncharacterized. In a multicenter study, we found that young people who experience significant complications related to BAV disease before age 30 are distinguished from the majority of BAV cases that manifest after age 50 by a relatively severe clinical course, with higher rates of surgical interventions, more frequent second interventions, and a greater burden of congenital heart malformations. These observations highlight the need for prompt recognition, regular lifelong surveillance, and targeted interventions to address the significant health burdens of patients with early-onset BAV complications.