Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by physical, psychological and physiological abnormalities. Obesity and related cardiovascular diseases are a common problem in adult patients with PWS. This report describes a case of adult PWS with heart failure associated with marked obesity and sleep-disordered breathing that was successfully treated with oxygen therapy, adaptive servoventilation, medications, diet therapy and rehabilitation
Prader-Willi Syndrome (PWS) is a genetically determined neurodevelopmental disorder occurring in 1 i...
Prader-Willi syndrome (PWS) is a complex genetic disorder affecting multiple body systems. It occur...
We describe the National Institutes of Health rare disease consortium for Prader-Willi syndrome (PWS...
Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the meta...
In Prader-Willi syndrome (PWS) adult patients, sleep-breathing disorders, especially obstructive sle...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is an imprinted genetic disorder conferred by loss of paternal gene expr...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Obesity, mild intellectual disability, hypotonia, poor sucking, cryptorchidism in males, hypogonadis...
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and fee...
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and fee...
Prader-Willi syndrome (PWS) is a disorder comprisingsevere neonatal hypotonia, hypogonadism, gross o...
With the advancement of medical care, the survival of most patients with syndromal genetic disease i...
Background: Prader-Willi syndrome is a severely disabling genetic condition. Treatments are availabl...
Background: Prader-Willi syndrome (PWS) is the most common known genetic cause of life-threatening o...
Prader-Willi Syndrome (PWS) is a genetically determined neurodevelopmental disorder occurring in 1 i...
Prader-Willi syndrome (PWS) is a complex genetic disorder affecting multiple body systems. It occur...
We describe the National Institutes of Health rare disease consortium for Prader-Willi syndrome (PWS...
Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the meta...
In Prader-Willi syndrome (PWS) adult patients, sleep-breathing disorders, especially obstructive sle...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is an imprinted genetic disorder conferred by loss of paternal gene expr...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Obesity, mild intellectual disability, hypotonia, poor sucking, cryptorchidism in males, hypogonadis...
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and fee...
Prader-Willi syndrome (PWS) is a genetic disorder which is characterized by severe hypotonia and fee...
Prader-Willi syndrome (PWS) is a disorder comprisingsevere neonatal hypotonia, hypogonadism, gross o...
With the advancement of medical care, the survival of most patients with syndromal genetic disease i...
Background: Prader-Willi syndrome is a severely disabling genetic condition. Treatments are availabl...
Background: Prader-Willi syndrome (PWS) is the most common known genetic cause of life-threatening o...
Prader-Willi Syndrome (PWS) is a genetically determined neurodevelopmental disorder occurring in 1 i...
Prader-Willi syndrome (PWS) is a complex genetic disorder affecting multiple body systems. It occur...
We describe the National Institutes of Health rare disease consortium for Prader-Willi syndrome (PWS...