Prader-Willi Syndrome Market Research Report 2018
Summary The latest Pharmaceutical and Healthcare disease pipeline guide Prader-Willi Syndrome (PWS) Pipeline Review, H2 2018, provides an overview of the Prader-Willi Syndrome (PWS) (Genetic Disorders) pipeline landscape. Prader-Willi Syndrome (PWS) is a rare genetic disorder present at birth that results in a number of physical, mental and behavioral problems. PWS is due to lack of several genes on one of an individuals two chromosome 15s. In the majority of cases, there is a deletion. In remaining cases, the entire chromosome from the father is missing and there are instead two chromosome 15s from the mother (uniparental disomy). Symptoms include poor muscle tone, low levels of sex hormones and a constant feeling of hunger. Report Highlights Prader-Willi Syndrome Market Research Report 2018