Updated: 11-04-2025
Prader-Willi Syndrome is a rare syndrome that occurs during birth and causes several behavioural, physical, and mental problems in the child.
Let us know more about Prader-Willi Syndrome: symptoms, treatment, and diagnosis.
A constant sense of wanting to eat that starts mostly around two years is a common feature of this type of syndrome.
Such people never feel full and always need something to eat, which makes it difficult for them to control their weight.
Obesity can lead to major health problems in patients with Prader-Willi syndrome.
Prader-Willi Syndrome: Symptoms, Treatment, Diagnosis
Symptoms of Prader-Willi Syndrome
Poor muscle tone, distinct facial features, poor sucking ability, lack of proper coordination in eyes, and poor responsiveness are some of the symptoms of this syndrome.
Diagnosis/Tests of Prader-Willi Syndrome
All or any of the above symptoms may cause your healthcare giver to recommend a blood test for detecting this type of disorder.
Treatment for Prader-Willi Syndrome
The children will need both treatment and care, such as:
- Good nutrition for newborns helps them gain weight
- Treatment of human growth hormone
- Sex hormonal treatment
- Treatment for sleep disturbances
- Treatment for overall development
- Overall mental care
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