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Bookmark or Share- Rett Syndrome | National Institute of Neurological Disorders ...Rett syndrome is a neurodevelopmental disorder. It is characterized by typical early growth and development, which is then followed by: A slowing of development. Loss of mobility or function in the hands. Distinctive hand movements. Slowed brain and head growth. Problems with walking, walking on the toes, or a wide-based gait. Seizures.
- What is Rett syndrome?What is Rett syndrome? Rett syndrome is a rare genetic neurological disorder that occurs almost exclusively in girls, more rarely in boys, and leads to severe impairments, affecting nearly every aspect of the child’s life: their ability to speak, walk, eat, and even breathe easily.
- Rett syndrome - WikipediaRett syndrome ( RTT) is a genetic disorder that typically becomes apparent after 6–18 months of age and almost exclusively in females. [4] Symptoms include impairments in language and coordination, and repetitive movements. [4] Those affected often have slower growth, difficulty walking, and a smaller head size.
- Rett syndrome - Symptoms & causes - Mayo ClinicRett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops. This disorder causes a progressive loss of motor skills and language. Rett syndrome primarily affects females. Most babies with Rett syndrome seem to develop as expected for the first six months of life.
- Rett Syndrome: What is it, Causes, Symptoms & TreatmentOverview. What is Rett syndrome? Rett syndrome is a rare neurodevelopmental (brain and nerve) disorder. Children with Rett syndrome appear to develop typically in the first year of life, but they lose the ability to use their hands purposefully. Other development then slows as they get older.
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