Prader-Willi Syndrome (PWS) is a genetic disorder caused by a lack of the 11q-13q segment of the paternal chromosome 15. Although the cause of the lack of genetic information varies, the result is an extreme increase in appetite, hypogonadism, mental retardation, and behavioral problems. Often, the most prominent obstacle the individual with PWS faces is managing the excessive weight gain that comes with having constant, ravenous hunger. Since there currently is no cure, managing the symptoms is the focus for most doctors. If the issue of excessive weight gain can be mollified, then the disorder would become more manageable. Therefore, I am proposing a hypothetical research project that examines the effects of capsaicin, a potential weight ...
International audiencePrader–Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involvi...
Prader-Willi syndrome (PWS) is a rare neurogenetic disorder characterised by hypotonia (especially p...
Prader⁻Willi syndrome (PWS) is a complex genetic disorder that, besides cognitive impairments, is ch...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the meta...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
A central characteristic of people with Prader-Willi Syndrome (PWS) is an apparent insatiable appeti...
Prader-Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of...
Prader–Willi syndrome (PWS) is a complex genetic disorder which involves the endocrine and neurologi...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Background This study reports a case of Prader Willi syndrome (PWS), a genomic imprinting disease re...
Prader-Willi syndrome (PWS) is a disabling condition characterized by hypotonia, hyperphagia, obesit...
International audiencePrader–Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involvi...
Prader-Willi syndrome (PWS) is a rare neurogenetic disorder characterised by hypotonia (especially p...
Prader⁻Willi syndrome (PWS) is a complex genetic disorder that, besides cognitive impairments, is ch...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the meta...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
A central characteristic of people with Prader-Willi Syndrome (PWS) is an apparent insatiable appeti...
Prader-Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of...
Prader–Willi syndrome (PWS) is a complex genetic disorder which involves the endocrine and neurologi...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Background This study reports a case of Prader Willi syndrome (PWS), a genomic imprinting disease re...
Prader-Willi syndrome (PWS) is a disabling condition characterized by hypotonia, hyperphagia, obesit...
International audiencePrader–Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involvi...
Prader-Willi syndrome (PWS) is a rare neurogenetic disorder characterised by hypotonia (especially p...
Prader⁻Willi syndrome (PWS) is a complex genetic disorder that, besides cognitive impairments, is ch...