With the advancement of medical care, the survival of most patients with syndromal genetic disease is greatly improved. In this case report, we have reported an adult Prader-Willi syndrome patient who is being diagnosed at the age of 33. The clinical features and their associated complications during adulthood have been reviewed
Clinical criteria for the diagnosis of Prader-Willi Syndrome (PWS) were established by consensus in ...
3noAlthough Prader-Willi syndrome is a rare disease, it provides an excellent example of how early ...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Background: Prader-Willi syndrome is a severely disabling genetic condition. Treatments are availabl...
The life expectancy of persons with PraderWilli syndrome (PWS) has increased in recent years. Becaus...
Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by physical, psychological and ...
Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the meta...
Prader-Willi syndrome is a rare genetic disease, characterized by hypothalamic-pituitary anomalies, ...
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 characterized by temper tantrums, impulsivity, mood fluctuations, dif...
Introduction: Adults with Prader-Willi syndrome (PWS) have an increased occurrence of several medica...
Background: Prader-Willi syndrome (PWS) is the most common known genetic cause of life-threatening o...
Prader-Willi syndrome (PWS) is a rare genetic syndrome, caused by the loss of expression of the pate...
Contains fulltext : 221496.pdf (Publisher’s version ) (Open Access
Clinical criteria for the diagnosis of Prader-Willi Syndrome (PWS) were established by consensus in ...
3noAlthough Prader-Willi syndrome is a rare disease, it provides an excellent example of how early ...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Background: Prader-Willi syndrome is a severely disabling genetic condition. Treatments are availabl...
The life expectancy of persons with PraderWilli syndrome (PWS) has increased in recent years. Becaus...
Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by physical, psychological and ...
Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the meta...
Prader-Willi syndrome is a rare genetic disease, characterized by hypothalamic-pituitary anomalies, ...
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 characterized by temper tantrums, impulsivity, mood fluctuations, dif...
Introduction: Adults with Prader-Willi syndrome (PWS) have an increased occurrence of several medica...
Background: Prader-Willi syndrome (PWS) is the most common known genetic cause of life-threatening o...
Prader-Willi syndrome (PWS) is a rare genetic syndrome, caused by the loss of expression of the pate...
Contains fulltext : 221496.pdf (Publisher’s version ) (Open Access
Clinical criteria for the diagnosis of Prader-Willi Syndrome (PWS) were established by consensus in ...
3noAlthough Prader-Willi syndrome is a rare disease, it provides an excellent example of how early ...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...