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

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

VYKAT XR was approved by the U.S. Food and Drug Administration (FDA) on March 26, 2025, and is now commercially available to ...

Relmada Therapeutics is a clinical-stage biotechnology company focused on developing transformative therapies for central nervous system and oncology-related conditions. Its lead candidates, NDV-01 ...

Announced U.S. Food and Drug Administration (FDA) approval of VYKAT XR (diazoxide choline) extended-release tablets, previously referred to as DCCR, for the treatment of hyperphagia in adults and ...

The former glamour model, 46, took to her Snapchat on Sunday to explain how 22-year-old's size was affecting his quality of life and putting him at risk of a heart attack.

Albinism is a rare genetic condition marked by little to none of the pigment melanin, which is responsible for the color in hair, skin, and the irises of the eyes. This results in a range of very ...

It occurs spontaneously in about 15,000 to 125,000 live births due to the deletion or lack of expression of a certain set of genes in chromosome 15 ... genetics of Prader-Willi syndrome are ...

the International Prader-Willi Syndrome Organization (IPWSO) and the Foundation for Prader-Willi Research (FPWR). PWS, which occurs in roughly 1 of every 15,000 live births, is caused by mutations in ...

Methylation studies for Prader-Willi syndrome were negative ... in the neonatal period. G-banded chromosome analysis demonstrated a de novo 46, XX, der(9)t(9;15)(p24.3;q25) karyotype.