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What is Rett syndrome?
May 3, 2022 · Rett syndrome is a rare genetic disorder that affects brain development and causes loss of skills, seizures and intellectual disabilities. Learn about the signs, stages and complications of this disorder and how it's diagnosed and treated.
May 6, 2021 · Rett syndrome is a rare genetic disorder that affects mostly girls and causes developmental delays, seizures and motor problems. Learn about the stages, diagnosis and management of this condition.
Rett syndrome is a rare genetic disorder that affects nearly every aspect of a child's life, causing severe impairments and repetitive hand movements. Learn about the symptoms, causes, diagnosis and treatment of Rett syndrome from experts and parents at the International Rett Syndrome Foundation.
Aug 19, 2022 · Rett syndrome is a rare, severe, and progressive disorder that affects mostly girls. It can impact your child’s ability to speak, walk, eat, or breathe easily. Learn about the signs, stages, diagnosis, and outlook of this condition.
Nov 28, 2023 · Rett syndrome is a neurodevelopmental disorder that affects mostly girls and is caused by a mutation in the MECP2 gene. It causes developmental regression, seizures, motor problems, and other symptoms that vary in severity and age of onset.
Rett syndrome is a rare genetic disorder that affects brain development and causes loss of muscle tone, speech, coordination, and other abilities. Learn about the typical and associated symptoms, stages, and complications of Rett syndrome from the National Institute of Child Health and Human Development.
Rett syndrome (RTT) is a genetic disorder that typically becomes apparent after 6–18 months of age and almost exclusively in females. Symptoms include impairments in language and coordination, and repetitive movements. [4]
