What are the characteristics of Willy syndrome

There is no cure for Willy syndrome. It can only be temporarily improved through some methods. It will also completely affect the patient's height, making the patient very short and unable to grow taller. Even the facial features are different from other people. Some patients will also affect the size of their reproductive organs. If the patient is a male, it will lead to very poor sperm quality, which will affect fertility to a certain extent, resulting in a very unique situation.

feature

In addition to a voracious appetite, patients with Prostatitis are also short in stature, lazy in exercise, weak muscles, and slow metabolism; their hands, feet, and genitals are small; their mouths are a distinctive triangle; their eyes are almond-shaped; and they habitually bite their nails. Most patients are thin and pale and have poor learning ability. The cause of this disease is very special. Unlike other genetic diseases, Prof. Pfizer's disease is not inherited. It is a gene deficiency produced during the egg (sperm) or embryo formation stage, that is, more than 10 genes are omitted or suppressed on the long strand of chromosome 15. At least 10 abnormal genes are associated with Prof.

Prader-Willi syndrome (PWS) is characterized by intrauterine hypotonia, intellectual disability, and hypogonadotropic hypogonadism. PWS is caused by deletions of paternally expressed genes within the PWS critical region on chromosome 15q, including a small nuclear ribonucleoprotein. However, the exact metabolic function of the deleted gene is unclear. A major difference in obesity in PWS is that ghrelin levels are elevated, whereas in other forms of obesity they are decreased. Gleevecrin, a gastric protein, may be at least partially responsible for the excessive appetite seen in PWS.

The most common behaviors reported are compulsive behaviors, such as scratching the skin, repeatedly asking questions, and collecting objects and repeatedly rearranging them. They tend to be stubborn and stubborn; many have exceptional memories or special skills in certain areas, such as puzzles. The gene that afflicts people with Prader-Willi syndrome is also related to the function of the hypothalamus, one of the first areas of the brain to be discovered. The hypothalamus transmits hormonal responses and controls metabolic systems such as heart rate, body temperature, and human growth.