Prader–Willi syndrome

Prader–Willi syndrome is a rare genetic disorder. It causes obesity, slow sexual development and low intelligence. People with Prader–Willi syndrome also have a higher chance of getting diabetes mellitus, and cannot have children. They are hungry very often, and eat much more than other people. It was first described in 1956.^[2] Prader-Willi syndrome is usually diagnosed with a genetic test. Prader-Willi syndrome has no cure. It can be treated with behavioural therapy.

References[change | change source]

↑ Mary Jones. "Case Study: Cataplexy and SOREMPs Without Excessive Daytime Sleepiness in Prader Willi Syndrome. Is This the Beginning of Narcolepsy in a Five Year Old?". European Society of Sleep Technologists. Retrieved April 6, 2009.
↑ "Prader-Labhardt-Willi syndrome". Whonamedit. Archived from the original on August 21, 2016. Retrieved 28 December 2022.

This short article about biology can be made longer. You can help Wikipedia by adding to it.

[1] Mary Jones. "Case Study: Cataplexy and SOREMPs Without Excessive Daytime Sleepiness in Prader Willi Syndrome. Is This the Beginning of Narcolepsy in a Five Year Old?". European Society of Sleep Technologists. Retrieved April 6, 2009.

[Name2016-2] "Prader-Labhardt-Willi syndrome". Whonamedit. Archived from the original on August 21, 2016. Retrieved 28 December 2022.

[1]

[2]