Rett Syndrome

Rett Syndrome, a neurological disorder named after Dr. Andreas Rett, who first described the condition, it occurs predominantly in girls. 
The child with Rett syndrome usually shows an early period of normal or near-normal development until about 6 to 18 months of age. 
A period of temporary stagnation or regression follows during which time the child loses communication skills and purposeful use of the hands.  Soon, stereotyped hand movements, gait disturbances, and slowing of the rate of head growth become apparent. 
Other problems encountered may include seizures and disorganized breathing patterns.  Apraxia, the inability to program the body to perform motor movements, is the most fundamental and severely handicapping aspect of Rett.  Rett is a developmental disorder rather than a degenerative disorder as once thought. 

In 1999, it was discovered that Rett syndrome is caused by a mutation of the MECP2 gene on the X chromosome. 
Now that the gene has been found, new efforts are underway to develop treatments and ultimately a cure, for Rett syndrome.

We hope to serve as a support system for families and professionals

• To promote an awareness and understanding of Rett syndrome
• To promote research of Rett syndrome
• To promote the general welfare of those whose lives are affected by Rett syndrome
• To host conferences, workshops and support group meetings
• To publish a newsletter
• To collect and disseminate information about Rett syndrome