14 нояб. 2024 г. · This rare genetic condition leads to physical, mental and behavioral problems, including being hungry all the time. |
Prader-Willi syndrome (PWS) is a recognizable syndromic form of neurodevelopmental disorder. It is the most common congenital imprinting disease. |
Brief Overview of PWS. • PWS is a very complex, neurobehavioral, genetic disorder caused by an abnormality on the 15th chromosome. |
Prader-Willi syndrome is a rare genetic condition that causes a wide range of physical symptoms, learning difficulties and behavioural challenges. |
Prader-Willi syndrome (PWS) is characterised by short stature, small hands and feet, an abnormal body composition (reduced lean tissue and increased fat ... |
Prader-Willi syndrome (PWS) is a complex genetic disorder with many manifestations and potential medical and psychiatric complications. |
Prader-Willi syndrome (PWS) is a complex hypothalamic disorder, combining hyperphagia, hypotonia, intellectual disability, and pituitary hormone deficiencies. |
Most adults with Prader-Willi syndrome are not able to live fully independent lives, such as living in their own home and having a full-time job. This is ... |
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