Doctors do not diagnose the girl rare genetic anomaly, because the child seemed to them too beautiful for this disorder. The girl's mother had to find answers to their questions Internet.
Angelman Syndrome
Englishwoman Melissa Adams was born with
syndrome Angelman - A rare genetic anomaly, which is characterized by delay mental development, sleep disturbance, seizures, chaotic traffic, regular laugh or smile. Often victims of this disorder can not say that It happened with Melissa, which remains silent to 10 years
children's disease
Angelman Syndrome It occurs in one child every 25 000. The girl's mother spent years in dealing with doctors who persistently talked her that her daughter very well. Katherine Adams realized that her Melissa something not when she was just a year. "Melissa cried all the time - the woman said. - She could not lie down on his stomach, I did not want to sit without It makes no sound, which usually say kids. She did not have desires with someone to chat. "
Angelman Syndrome
Dozens of times a woman led Melissa to the doctors, but they otfutbolivat it back, saying that the child is "too beautiful" to to suffer from some developmental disorders. In two years, she finally put diagnosed with autism, which proved to be erroneous. After that, the mother decided to appeal Internet. She hammered symptoms daughter into a search engine, and he immediately gave her Angelman Syndrome. However, doctors do not believe in the diagnosis and sent back mother and daughter home. Just a trip to the other children's hospital located 100 km from the house, and genetic analysis confirmed the assumption mother.
"I had mixed emotions - anger at doctors and relief from the fact that I know the name of the disease, "- says Katherine. In Currently, no treatments for Angelman syndrome is not, although being some research on this topic. (READ MORE)
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