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drMAHER
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Tuesday 14 April 2026 00:45:09 GMT
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Prader-Willi Syndrome (PWS) is a rare genetic condition that affects development, metabolism, and behavior. It is caused by a problem with genes on chromosome 15, usually due to missing or inactive genetic material. In early infancy, people with PWS often have low muscle tone and feeding difficulties. As they grow, this typically shifts to an intense and persistent feeling of hunger (called hyperphagia), which can lead to overeating and obesity it not caretully managea. Individuals with PWS may also experience learning difficulties, short stature, and hormonal imbalances. While there is no cure, treatment focuses on managing symptoms such as strict food supervision, growth hormone therapy, and supportive care to help improve quality of life.
Prader-Willi Syndrome (PWS) is a rare genetic condition that affects development, metabolism, and behavior. It is caused by a problem with genes on chromosome 15, usually due to missing or inactive genetic material. In early infancy, people with PWS often have low muscle tone and feeding difficulties. As they grow, this typically shifts to an intense and persistent feeling of hunger (called hyperphagia), which can lead to overeating and obesity it not caretully managea. Individuals with PWS may also experience learning difficulties, short stature, and hormonal imbalances. While there is no cure, treatment focuses on managing symptoms such as strict food supervision, growth hormone therapy, and supportive care to help improve quality of life.
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#turkey #istanbul🇹🇷❤️ #turquia #foryoupage #foryour

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