Rett Syndrome Causes, Symptoms, Stages, Treatment

Rett syndrome is a rare genetic neurological and developmental disorder that affects how the brain develops. This disorder results in a progressive loss of motor and language skills.

What are the Causes of Rett Syndrome?

Rett syndrome is caused by random genetic changes, most commonly in the MECP2 gene. The genetic changes appear to cause issues with protein production, which is essential for brain development. However, the precise cause is still unknown and is being researched.

What are the Symptoms of Rett Syndrome?

For the first six months, most infants with Rett syndrome appear to grow and behave normally. Following that, signs and symptoms begin to emerge.

The main signs and symptoms include Slowed growth, Loss of movement and coordination abilities, Loss of communication abilities, Breathing problems and Seizures.

What are the Stages of Rett Syndrome?

Rett syndrome is typically classified into four stages: Early onset, Rapid deterioration, Plateau and Late motor deterioration

Can Rett Syndrome be treated?

Treatments for Rett syndrome in children and adults include: Regular medical care,  Medications, Physical therapy and Nutritional support