Prader-Willi Syndrome NFZ — 17 facilities in 16 cities

Prader-Willi syndrome is a rare genetic disorder presenting with neonatal hypotonia, followed by uncontrolled appetite leading to obesity, growth hormone deficiency, developmental delay, and behavioral issues. NFZ covers genetic testing, growth hormone therapy to improve body composition and growth, and multidisciplinary care including endocrinology, dietetics, and rehabilitation.