Prader-Willi (PRAH-dur VIL-e) syndrome is a rare genetic disorder that results in a number of physical, mental and behavioral problems. A key feature of Prader-Willi syndrome is a constant sense of hunger that usually begins at about 2 years.
inzulin. Čeprav so nekateri zapleti pri otrocih in mladostnikih manj pogosti kot pri odraslih (npr. sladkorna bolezen tipa 2), pa glede na naravni potek debelosti lahko pričakujemo, da se bodo tudi ti pojavljali vse bolj zgodaj in pomembno povečali obolevnost in umrljivost celotne populacije. Ob tem na kakovost življenja.
(1)Department of Endocrinology, Nationwide Children's Hospital, Columbus, OH, Prader-Willi syndrome (PWS) is a complex genetic disorder with implications .
Apr 5, 2019 Prader-Willi syndrome (PWS) is a genetic disorder that can lead to obesity, and nutritionists have long histories of treating patients.
Researchers have uncovered new insights into the brain mechanisms underlying the insatiable hunger and subsequent obesity in patients with Prader-Willi syndrome. A study published in the journal.
BACKGROUND: Prader-Willi syndrome (PWS) is a rare genetic disorder with an associated anomaly in chromosome 15, and has been reported to increase .