Rett syndrome

Other development then slows as they get older. Rett syndrome is a rare genetic neurological disorder that occurs primarily in girls and more rarely in boys.

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Its related to autism spectrum disorder.

. Rett syndrome is a rare childhood neurological and developmental disorder that almost exclusively affects females. Loss of muscle tone slowing of development difficulty feeding jerkiness in arm and leg movement. Rett syndrome is a neurodevelopmental condition that primarily affects girls.

Rett syndrome is a rare neurodevelopmental brain and nerve disorder. Babies with Rett syndrome seem to grow and develop normally at first. Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops.

Rett syndrome RTT is a genetic disorder that typically becomes apparent after 618 months of age in females. 3 Symptoms include impairments in language and coordination and repetitive movements. People with the disease appear to have normal psychomotor development during the first 6 to 18 months of life followed by a developmental plateau.

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. Rett syndrome causes developmental challenges throughout childhood. Children with Rett syndrome appear to develop typically in the first year of life but they lose the ability to use their hands purposefully.

This disorder causes a progressive loss of motor skills and language. The hallmark of Rett. Rett syndrome is a progressive neuro-developmental condition that primarily affects girls.

Rett syndrome leads to severe impairments affecting nearly every aspect of the childs life. Finding trusted information is the first step towards simplifying this journey. 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.

Most babies with Rett syndrome seem to develop as expected for the first six months of life. Between 3 months and 3 years of age though they stop developing and even lose some skills. Rett syndrome is a rare genetic disease that causes developmental and nervous system problems mostly in girls.

Infants appear to develop normally for the first several months before development stalls typically between the ages of 6-18 months. 3 Those affected often have slower growth difficulty walking and. Their ability to speak walk eat and even breathe easily.

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 primarily affects females. Rett syndrome is a neurodevelopmental disorder that affects girls almost exclusively.

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