What is the life Expectancy for Rett Syndrome?

Rett syndrome is a rare, genetic, neurodevelopmental disorder that affects brain development.

This disorder causes progressive loss of motor and language skills. Females are disproportionately affected by Rett syndrome.

While it is known that Rett syndrome reduces lifespan, little is known about specific Rett syndrome life expectancy rates.

Death is sudden and often secondary to pneumonia. Patients can often survive into their 40s or 50s with proper care, including nutrition as well as physical and occupational therapies.

For the first six months of life, most babies with Rett syndrome appear to develop normally.

Children with Rett syndrome gradually develop difficulties with the use of muscles that control movement, coordination, and communication.

Although there is currently no cure for Rett syndrome, potential treatments are being investigated.

Current treatment focuses on improving movement and communication, treating seizures, and providing care and support to children, adults, and their families with Rett syndrome.