Rett syndrome

Rett syndrome RTT is a genetic disorder that typically becomes apparent after 618 months of age in females. Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops.

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3 Symptoms include impairments in language and coordination and repetitive movements.

. 3 Those affected often have slower growth difficulty walking and a. Rett syndrome leads to severe impairments affecting nearly every aspect of the childs life. 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.

Most babies with Rett syndrome seem to develop as expected for the first six months of life. Rett syndrome is a rare childhood neurological and developmental disorder that almost exclusively affects females. 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 progressive neurodevelopmental disorder that affects a childs brain development and cognitive ability. 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 progressive neuro-developmental condition that primarily affects girls.

Rett syndrome is a rare neurodevelopmental brain and nerve disorder. This disorder causes a progressive loss of motor skills and language. Rett syndrome is a neurodevelopmental disorder that affects girls almost exclusively.

The hallmark of Rett syndrome is near constant repetitive hand movements. Finding trusted information is. People with the disease appear to have normal psychomotor development during the first 6 to 18 months of life followed by a developmental plateau.

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. Rett syndrome causes developmental challenges throughout childhood.

Loss of muscle tone slowing of development difficulty feeding jerkiness in arm and leg movement. Infants appear to develop normally for the first several months before development stalls typically between the ages of 6-18 months. Rett syndrome is a neurodevelopmental condition that primarily affects girls.

Rett syndrome primarily affects females. 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. Over time it can cause severe problems with language and communication lack of coordination and muscle control.

Their ability to speak walk eat and even breathe easily.

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