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Related websites
Rett syndrome - Wikipedia
WEBrett 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]
En.wikipedia.orgRett syndrome - Symptoms & causes - Mayo Clinic
WEBMay 3, 2022 · rett 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.
Mayoclinic.orgWhat is Rett syndrome?
WEBrett 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.
Rettsyndrome.orgOntario Rett Syndrome Association | O.R.S.A. – rett
WEBWhat is rett Syndrome? rett syndrome (RTT) is a rare genetic neurological disorder that occurs almost exclusively in females; even rarer in males. It is estimated that 1 in 10,000 are affected by RTT, usually caused by a mutation of the MECP2…
Rett.caHomepage - International Rett Syndrome Foundation
WEBWhat is rett Syndrome? rett syndrome is a rare genetic neurological disorder that leads to severe impairments, affecting nearly every aspect of life. rett particularly affects speech, purposeful hand use, and coordination, leaving individuals understanding more than they can communicate.
Rettsyndrome.orgRett Syndrome: What is it, Causes, Symptoms & Treatment - Cleveland Clinic
WEBMay 6, 2021 · 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.
My.clevelandclinic.orgRett Syndrome - National Institute of Neurological Disorders and Stroke
WEBrett syndrome is a neurodevelopmental disorder characterized by typical early growth and development 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, seizures, cognitive problems, digestive problems, and other symptoms.
Ninds.nih.govAbout Rett Syndrome - International Rett Syndrome Foundation
WEBrett syndrome is a rare genetic neurological disorder that affects 1 in 10,000 females (and even more rarely in males) and begins to display itself in missed milestones or regression at 6-18 months.
Rettsyndrome.orgRett Syndrome Symptoms, Causes, and Treatments - WebMD
WEBAug 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. Parents or doctors usually notice
Webmd.comRett syndrome - Diagnosis & treatment - Mayo Clinic
WEBMay 3, 2022 · Diagnosis of classic rett syndrome includes these core symptoms, which may start to show up anytime from 6 to 18 months of age: Partial or complete loss of purposeful hand skills. Partial or complete loss of spoken language. Walking problems, such as difficulty walking or not being able to walk.
Mayoclinic.org