Juliana Steffan's mother, April Steffan, created a YouTube video about Prader-Willi syndrome, a rare genetic disorder that causes a chronic feeling of hunger, among other physical, mental and ...

CHATHAM, N.J., Feb. 11, 2021 (GLOBE NEWSWIRE) -- Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the Company), a clinical-stage biopharmaceutical company, today announced an agreement ...

Patients with Prader-Willi syndrome showed early signs of microvascular disease upon screening. In a study using urinalysis screening to detect microvascular disease, 1 in 5 adults with Prader-Willi ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized cutting-edge findings on Prader-Willi syndrome (PWS), revealing how this complex ...

Tesomet is an investigational fixed-dose combination therapy of tesofensine, a triple monoamine reuptake inhibitor, and metoprolol, a beta-1 selective blocker. The Food and Drug Administration (FDA) ...

(Reuters) -The U.S. Food and Drug Administration on Wednesday approved Soleno Therapeutics' drug to treat a rare genetic disorder, making it the first treatment available for patients who experience ...

Certain rare genetic disorders may cause a child to develop obesity. Health experts may refer to these conditions as syndromic childhood obesity. They may affect a child’s metabolism or cause them to ...

Walk through Elizabeth Bystrak's sunny home in Orchard Park, and you'll notice an unusual floor plan. There's a dining room, an open-plan kitchen. And then there's a separate area -- behind a locked ...

REDONDO BEACH, Calif., Sept. 20, 2017 /PRNewswire-USNewswire/ -- Prader-Willi California Foundation will host its annual state conference to educate families and professionals caring for a child or ...

Please provide your email address to receive an email when new articles are posted on . The FDA granted orphan drug designation to an investigational drug for the treatment of Prader-Willi syndrome, ...