Results for: Genetic Disorder

The Prader-Willi syndrome (PWS) market is anticipated to experience significant growth in the coming years, fueled by rising diagnosis rates and the impending launch of innovative therapies. This rare genetic disorder affects individuals from birth, presenting challenges in areas such as muscle tone, development, and behavior, often leading to obesity if left unmanaged. This report delves into the current treatment landscape, emerging drugs, market dynamics, and future growth projections for the PWS market.

Cornelia de Lange Syndrome (CdLS) is a rare genetic disorder that can lead to distinctive facial deformities, growth deficiencies, and developmental delays. It is often caused by a mutation in the NIPBL gene, but can also be inherited from parents. This disorder can lead to discrimination and loneliness, which is why International Cornelia de Lange Syndrome (CdLS) Awareness Day is observed every year to raise awareness and understanding of the challenges faced by those affected by CdLS.