Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Syndromic disease · Complex neurodevelopmental disorder · Congenital nervous system disorder · Chromosomal disorder · Mendelian neurodevelopmental disorder · Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome · Congenital hypogonadotropic hypogonadism
Prader-Willi syndrome
Prader-Willi syndrome is a rare genetic disorder characterized by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioral problems or severe psychiatric problems.
-
Schaaf-Yang syndrome 0 trials