Rett syndrome

3 Those affected often have slower growth difficulty walking and. Rett syndrome is a complex neurological and developmental disorder in which early growth and development appear normal at first but then the infant stops developing and affected children even lose skills and abilities.

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Rett syndrome is a rare childhood neurological and developmental disorder that almost exclusively affects females.

. 3 Symptoms include impairments in language and coordination and repetitive movements. Rett syndrome RTT is a genetic disorder that typically becomes apparent after 618 months of age in females. Over time it can cause severe problems with language and communication lack of coordination and muscle control.

This disorder causes a progressive loss of motor skills and language. Rett syndrome is a rare neurodevelopmental brain and nerve disorder. Rett syndrome primarily affects females.

Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops. 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 neurodevelopmental disorder that affects girls almost exclusively.

Rett syndrome leads to severe impairments affecting nearly every aspect of the childs life. Loss of muscle tone slowing of development difficulty feeding jerkiness in arm and leg movement. Rett syndrome is a rare genetic neurological disorder that occurs primarily in girls and more rarely in boys.

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 is a progressive neurodevelopmental disorder that affects a childs brain development and cognitive ability. Other development then slows as they get older.

Rett syndrome is a neurodevelopmental condition that primarily affects girls. 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.

Finding trusted information is the first step towards simplifying this journey. Over time the effects of Rett syndrome can lead to cognitive sensory emotional. Most babies with Rett syndrome seem to develop as expected for the first six months of life.

The hallmark of Rett. Infants appear to develop normally for the first several months before development stalls typically between the ages of 6-18 months. Their ability to speak walk eat and even breathe easily.

1 Rett syndrome occurs mostly in females. People with the disease appear to have normal psychomotor development during the first 6 to 18 months of life followed by a developmental plateau.

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