Apa Itu Prader Willi Syndrome

Apa Itu Prader Willi Syndrome. More information on early detection for the best health outcome. Commonly associated characteristics of this disorder include diminished fetal activity, obesity, hypotonia.

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This leads to a number of problems and is thought to affect part of the brain called the hypothalamus, which produces hormones and regulates growth and appetite. Commonly associated characteristics of this disorder include diminished fetal activity, obesity, hypotonia. Pws affects males and females with equal frequency and affects all races and ethnicities.

Oleh karena itu, bayi yang lahir dalam keluarga dengan riwayat mengalami sindrom prader willi memiliki risiko lebih tinggi untuk mengidap.

It stems from a problem with one of your chromosomes your child's doctor should screen for scoliosis, hip dysplasia, or thyroid problems. The symptoms of prader‐willi syndrome are likely due to dysfunction of a portion of the brain called the hypothalamus. Explore symptoms, inheritance, genetics of this condition. In newborns, symptoms include weak muscles, poor feeding, and slow development.