Rett syndrome

Rett syndrome is a neurodevelopmental condition that 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.

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These babies then lose skills.

. Those affected often have slower growth difficulty walking and a smaller head size. Our unwavering strategy focuses on treatment medications gene therapy and neuro-habilitative therapies and we are bringing the first and only treatment that addresses the underlying biology for Rett syndrome into the final phase of. Rett syndrome is a progressive neurodevelopmental disorder that affects a childs brain development and cognitive ability.

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 genetic neurological disorder that occurs almost exclusively in girls and leads to severe impairments affecting nearly every aspect of the childs life. Over time it can cause severe problems with language and communication lack of coordination and muscle control involuntary hand movements and slowed growth.

This disorder causes a progressive loss of motor skills and language. Rett syndrome almost exclusively affects females although. What is Rett syndrome.

Other development then slows as they get older. Infants appear to develop normally for the first several months before development stalls typically between the ages of 6-18 months. 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 causes developmental challenges throughout childhood. Rett syndrome is an incredibly complex disorder that will require a multi-pronged approach to treat and cure. Rett syndrome primarily affects females.

1 Rett syndrome occurs mostly in females. Rett syndrome is a rare neurodevelopmental brain and nerve disorder. Rett syndrome RTT is a genetic disorder that typically becomes apparent after 618 months of age in females.

Rett syndrome is a neurodevelopmental disorder that affects girls almost exclusively. Rett syndrome is a rare childhood neurological and developmental disorder that almost exclusively affects females. Their ability to speak walk eat and even breathe easily.

Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops. Most babies with Rett syndrome seem to develop as expected for the first six months of life. 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.

Loss of muscle tone slowing of development difficulty feeding jerkiness in arm and leg movement. Symptoms include impairments in language and coordination and repetitive movements. The hallmark of Rett syndrome is near constant repetitive hand movements.

Over time the effects of Rett syndrome can lead to cognitive sensory emotional.

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