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Rett syndrome (RTT) is a neurodevelopmental disorder that occurs almost exclusively in females.
The most common form of the condition is known as classic Rett syndrome.After birth, girls with classic Rett syndrome have 6 to 18 months of apparently normal development before developing severe problems with language and communication, learning, coordination, and other brain functions. Treatment for Rett syndrome includes:
Rett Syndrome Pictures Rett's Syndrome - Neurological Examination, Presentation and Parent Interview - Duration: 12:28. It was described in 1966 by Andreas Rett, an Austrian pediatrician and neurologist [].After a brief period of initially normal development, affected patients experience loss of speech and purposeful hand use, stereotypic hand movements, and gait abnormalities. Infants with Rett syndrome seem to grow and develop normally at first, but then they stop developing and even lose skills in different stages of the disease over a lifetime. A defect in the MeCP2 gene on the X chromosome leads to the development of Rett syndrome.
See more ideas about Rett syndrome, Syndrome, Speech and language. Rett syndrome is a X-linked neurodevelopmental disorder affecting predominantly females in early childhood. Rett syndrome, rare progressive neurological disorder characterized by severe intellectual disability, autism-like behaviour patterns, and impaired motor function. The subtle signs can occur anytime between the six and eighteen months of age. The disorder was first described in the 1960s by the Austrian physician Andreas Rett. Rett syndrome Treatment. This condition is a … Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops, causing a progressive loss of motor skills and speech. May 10, 2020 - Explore romieh's board "Rett Syndrome", followed by 140 people on Pinterest. Girls with Rett syndrome survive due to the presence of two X chromosome as against boys who succumb to the disorder due to only one X chromosome in their body cells. Rett syndrome is commonly classified into four different stages. Rett Syndrome – Life Expectancy. The prevalence is estimated at 1.09 per 10,000 females by the age of 12 years (Laurvick et al. Cases of the syndrome were first described by Andreas Rett in 1966, with additional cases reported in the 1980s, leading to widespread recognition of Rett syndrome in the medical community. It is the early stage of the syndrome when you overlook the symptoms or signs. This disorder primarily affects girls. It is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability. Rett syndrome is a brain disorder that occurs almost exclusively in girls. Rett syndrome is a rare disorder which is primarily seen in girls.
On an average, the life expectancy is 45 to 50 years. Rett syndrome is a progressive, neuro-developmental condition that primarily affects girls. Affected girls appear to have normal psychomotor development during the first 6 to 18 months of life, followed by a developmental "plateau," and then rapid regression in language and motor skills. Thereafter the symptoms begin to cede.
INTRODUCTION.
Rett syndrome is related to autism spectrum disorder. The stages can describe the severity of the problem.
Rett syndrome Causes.