Tag: chromosome 15

  • Willi-Prader Syndrome

    Willi-Prader Syndrome

    Explore the complexities of Willi-Prader Syndrome (WPS), a rare genetic disorder linked to abnormalities on chromosome 15. This informative blog post delves into its causes, symptoms, and potential treatments, as well as personal stories that highlight the importance of early diagnosis and support for individuals and families affected by this condition. Discover how understanding WPS…

  • Prader Willi Syndrome

    Prader Willi Syndrome: Definition and Description of Prader Willi Syndrome: Prader Willi Syndrome (PWS) is a complex genetic disorder characterized by a range of symptoms including hypotonia (poor muscle tone), obesity, cognitive impairment, and behavioral issues. PWS is caused by the loss of function of specific genes on chromosome 15, which typically occurs due to…

  • Prader-Labhart-Willi Fancone Syndrome

    Prader-Labhart-Willi Fancone Syndrome: Definition and Description of Prader-Labhart-Willi Fancone Syndrome: Prader-Labhart-Willi Fancone Syndrome (PLWFS) is a rare neurogenetic disorder characterized by a combination of symptoms that significantly impact both physical and cognitive aspects of individuals affected by it. This syndrome is associated with genetic anomalies that occur due to the deletion of specific genes on…