Long-term clinical profiles of female patients with classic Rett syndrome are presented and exemplified by three cases, as experienced over four decades. Emphasized is the frequently surprisingly ...

Rett syndrome is a rare genetic neurological disorder that almost exclusively occurs in girls. It leads to serious impairments that affect almost every part of the child's life. Though Rett ...

She has Rett syndrome, a complex neurological disorder ... Clare would forever have the understanding of a baby. I have always doubted that assumption. Clare's eyes are wise, warm and expressive.

Rizzo is diagnosed with Rett syndrome, which leads to a regression of basic skills that a small child may have already learned. Her parents say that the volunteers at Sebastian Riding Associates ...

New discoveries about the severe developmental disorder known as Rett syndrome could open the door to better treatments for the devastating, life-shortening condition. Scientists investigating the ...

there is a risk of unnecessary negative side effects in the all-too-premature aging process associated with Rett syndrome. With regard to epileptic seizures, the paroxysmal vacant spells described ...

Scientists investigating the severe developmental disorder known as Rett syndrome have discovered a series of crucial molecular changes that occur long before symptoms appear. The findings could ...

If you haven't heard of Rett syndrome, it's probably because it's very rare. Affecting an estimated one in 12,000 baby girls born each year (and only rarely seen in boys), this genetic disorder ...

Kemry Smith, a Utah girl, passed away from Rett syndrome, a rare disorder. Her mother, Natalie Smith, described Kemry as kind, caring and emotionally intuitive. Family, friends, and strangers ...

The Rett Center at Baylor is one of the few centers in the United States that specializes in the diagnosis and care of children and adults with Rett Syndrome. We provide care not only for those living ...

The resulting discord in gene expression leads to Rett syndrome. "In the current study, our goal was to better understand the molecular changes that occur upon loss of MeCP2 function. Previous ...