In December 2024, Nobias Therapeutics announced that the FDA had granted rare pediatric disease designation (RPDD) and orphan drug designation (ODD) to the company’s small-molecule metabotropic ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate cardiac development ... co-first author. DiGeorge syndrome, a 22q11.2 ...

27, 2025 — Heart disease remains the leading cause of death ... uncovered a potential reason why patients with Loeys-Dietz syndrome, an inherited connective tissue disorder, ...

Heart disease is a term used to describe a constellation of conditions that can affect the heart and/or its valves, vessels, structure, electrical system, or coronary arteries. Though each disease ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate cardiac development ... Center at Houston DiGeorge syndrome, a 22q11.2 ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate cardiac development ... co-first author. DiGeorge syndrome, a 22q11.2 ...

Correspondence to Dr Nathalie Auger, University of Montreal Hospital Centre Research Centre, Montreal H2P 1E2, Canada; nathalie.auger{at}inspq.qc.ca Background Patients with heart defects are at risk ...

Common types of congenital heart defects include Atrial Septal Defect (ASD), Ventricular Septal Defect (VSD), Tetralogy of Fallot, Coarctation of the Aorta, and Hypoplastic Left Heart Syndrome. How ...

The AI also gave doctors more confidence, allowing them to evaluate scans more quickly FRIDAY, Jan. 31, 2025 -- Artificial intelligence (AI) can help doctors detect fetal heart defects, improving ...

Artificial intelligence can help doctors detect fetal heart defects, improving newborns' chances of survival, a new study says. AI-aided analysis of prenatal ultrasounds detected heart defects ...