Rett syndrome

However there is an increased risk of sudden death in people with Rett syndrome. It is estimated to affect about 1 in 12000 girls born each year and is only rarely seen in boys.

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

. Rett syndrome is a neurodevelopmental condition that primarily affects girls. Over time it can cause severe problems with language and communication lack of coordination and muscle control. Children with Rett syndrome appear to develop typically in the first year of life but they lose the ability to use their hands purposefully.

Diagnosing Rett syndrome involves careful observation of your childs growth and development and answering questions about medical and family history. Signs and symptoms Some children with Rett syndrome are affected more severely than others. Their ability to speak walk eat and even breathe easily.

What is Rett syndrome. This condition mostly affects females but its still rare affecting only. Rett syndrome was first reported by Dr.

The most common form of the condition is known as classic Rett syndrome. Rett syndrome is a progressive neuro-developmental condition that primarily affects girls. Other development then slows as they get older.

The diagnosis is usually considered when slowing of head growth is noticed or loss of skills or developmental milestones occurs. Osteopenia can result in weak fragile bones. Infants appear to develop normally for the first several months before development stalls typically between the ages of 6-18 months.

Hindawis Academic Journals Are Peer-Reviewed Open Access. Ad Complexity Publishes Research And Review Articles across a broad range of disciplines. Many people with Rett syndrome live well into adulthood although they may require constant care and supervision.

Loss of muscle tone slowing of development difficulty feeding jerkiness in arm. Rett syndrome is a genetic disorder that appears in infancy and leads to significant physical and mental disabilities. 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 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. Rett syndrome is a brain disorder that occurs almost exclusively in girls. The hallmark of Rett syndrome is near constant repetitive hand movements.

For a diagnosis of Rett syndrome other conditions with similar. 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 is a rare neurodevelopmental brain and nerve disorder. Approximately one quarter of deaths in Rett are sudden and unexpected. Rett syndrome is a rare genetic disorder that affects brain development resulting in severe mental and physical disability.

Andreas Rett in 1966. 1 Rett syndrome occurs mostly in females. Rett syndrome is a progressive neurodevelopmental disorder that affects a childs brain development and cognitive ability.

Rett syndrome causes developmental challenges throughout childhood. 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. 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.

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