Angelman syndrome is a disease of genetic origin that affects the development of the child, leading to disorders of learning, speech as well as behavior which translates to a retardation of development. The symptoms of this condition begin to be visible from the year, moment in which signals physical as well as psychological are presented more clearly. But what characterizes children with this condition?
Angelman syndrome occurs due to a mutation in chromosome 15, thus being genetic. It’s a disorder that causes a severe developmental delay, reason by which the child will present some general symptoms that include all patients who suffer from this condition, as well as other signals which may vary from one patient to another.
There are mental and physical symptoms that manifest in many patients with this condition. Other symptoms of Angelman syndrome may occur less frequently.
This condition can be diagnosed by genetic as well as neurological tests that will help determine the presence of disease. It is advisable to visit a neurologist if you suspect its existence, because the immediate medical attention could help prevent seizures.
Occupational therapy as well as behavioral can help improve some of the symptoms of this condition, while physiotherapy improves the movement problems, however there is no cure for Angelman Syndrome.
This article is purely informative, in Dinzie we have no power to prescribe any medical treatment or perform any type of diagnosis. We invite you to see a physician in the case to present any kind of condition or malaise.