What is Rett syndrome?

Rett syndrome is a rare disorder that is probably seen in girls. Andreas Rett first described the cases of syndrome in 1966, with other cases reported in the 80s, which led to extensive recognition of Rett's syndrome in the medical community. This condition is a sexual disorder that includes errors on X chromosome, and it is much more common in girls than boys, mainly because male fruits with retic syndrome usually die before birth. In very rare cases, a mother with a slight housing, which is asymptomatic, can pass the damaged chromosome x to the infant, leading to the inherited case of Rett's syndrome. Genetic testing can confirm the diagnosis of Rett's syndrome, although the symptoms are usually sufficient for the physician to make a confident diagnosis.

There are four phases in this state. During early development, the child is normal and achieves expected developmental milestones and behaves as expected. In the early start phase, however, the child begins to have muscle coordination and may show earlySigns of what may seem like autism. The early onset of Rett's syndrome usually occurs between six and 18 months and the condition may not be diagnosed first because the symptoms are fine.

In the rapid destructive phase, the patient begins to experience extreme developmental and neurological problems that include slowing the growth of hands, legs and heads. The patient may develop cardiac abnormalities, seizures, muscle weakness, respiratory problems, scoliosis, growing lack of coordination and behavior problems. Some patients remain non -verbal.

During the plateau phase, the patient reaches a relatively stable point without further tasting or procedure. Finally, in the late deterioration of the RETT syndrome engine, the patient begins to have serious mobility problems. Knowledge can improve slightly during this phase.

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Rett syndrome cannot be cured but there are treatment that can be used to control the condition and to maintainPatient comfort. Treatment revolves around the treatment of symptoms, as they appear and provide professional, physical and psychological therapy to the patient to improve socialization and motor skills. The severity of the RETT syndrome may vary, as in many genetic conditions, depending on individual variations in the patient. Some patients are seriously disturbed, while others can enjoy normal functions; In all cases, therapy can help the patient live a more active and happier life.