Rett Syndrome
People with the disease appear to have normal psychomotor development during the first 6 to 18 months of life followed by a developmental plateau. Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops.
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Children with Rett syndrome appear to develop typically in the first year of life but they lose the ability to use their hands purposefully.
. Rett syndrome is a rare neurodevelopmental brain and nerve disorder. Finding trusted information is the first step towards simplifying this journey. 3 Those affected often have slower growth difficulty walking and.
The hallmark of Rett. Rett syndrome is a neurodevelopmental disorder that affects girls almost exclusively. 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 rare genetic neurological disorder that occurs primarily in girls and more rarely in boys. Rett syndrome RTT is a genetic disorder that typically becomes apparent after 618 months of age in females. This disorder causes a progressive loss of motor skills and language.
Their ability to speak walk eat and even breathe easily. Rett syndrome primarily affects females. Most babies with Rett syndrome seem to develop as expected for the first six months of life.
Rett syndrome causes developmental challenges throughout childhood. 3 Symptoms include impairments in language and coordination and repetitive movements. Other development then slows as they get older.
Rett syndrome is a neurodevelopmental condition that primarily affects girls. Rett syndrome is a rare genetic neurological disorder that occurs almost exclusively in girls and leads to severe impairments affecting nearly every aspect of the childs life. Rett syndrome leads to severe impairments affecting nearly every aspect of the childs life.
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