Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

Awareness Month, which seeks to raise recognition and push for research of this rare genomic imprinting disorder. PWS is estimated to affect about one in 20 000 individuals1 yet, until now, people ...

The relentless hunger and associated behaviours significantly impact the quality of life for those with Prader-Willi syndrome ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized ...

This figure illustrates the genomic structure of the PWS critical region on chromosome 15 ... have synthesized cutting-edge findings on Prader-Willi syndrome (PWS), revealing how this complex ...

In a comprehensive Genomic Press Invited Expert Review, researchers from the University of Haifa have synthesized ...

The drug, to be called Vykat XR, treats hyperphagia, the hallmark symptom of the Prader-Willi syndrome, a genetic disorder caused by full or partial deletions on chromosome 15 that affect the ...

Prader-Willi syndrome is a rare genetic disorder caused by abnormalities in chromosome 15. Symptoms include low muscle tone, developmental delays, and behavioural challenges. Hyperphagia ...

Prader-Willi syndrome is stated to be a rare genetic neurodevelopmental disorder stemming from an abnormality on chromosome 15 gene expression. According to the company’s estimation, around ...