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Rett Syndrome: more books (46)

Keeping Katherine: A Mother's Journey to Acceptance by Susan Zimmermann, 2004-12-28

Grief Dancers: A Journey into the Depths of the Soul by Susan Zimmermann, 1996-10

A NEATS Analysis of Autism Spectrum Disorders by Ph.D., LICSW Jane F. Gilgun, 2009-11-23

What is PDD?: Pervasive developmental disorders in school age children a handbook for parents, teachers and concerned professionals by Richard Paul Morriss, 1993

lists with details

The Rett-Syndrome
Julia promotes the International rett syndrome Association . Whatis the rett syndrome? The International rett syndrome Association.
http://www.juliaroberts.de/x-rett.htm

Extractions: Rett Syndrome is a neurological disorder seen almost exclusively in females, and found in a variety of racial and ethnic groups worldwide. The child with Rett Syndrome usually shows an early period of apparently normal or near normal development until 6-18 months of life. A period of temporary stagnation or regression follows during which the child loses communication skills and purposeful use of hands. Soon, stereotyped hand movements, gait disturbances, and slowing of the rate of head growth become apparent. Please visit the homepage of the organisation to learn more about the Rett Syndrome and the efforts of the " International Rett Syndrome Association ". What´s Julia´s participation? Julia appears in a documentary about the Rett Syndrome titled "Silent Angels". The shooting took place in Seattle, Los Angeles, Baltimore and New York. Julia is narrator of the project. The documentary aim is to discuss Rett Syndrome through the eyes of several families and with the assisstence of geneticists and other researchers. At the moment there are only 4.178 Rett cases identified in the whole world. But it must be much more. This film wants to find those missing or misdiagnosed kids.
HBOT, Rett Syndrome, & Cerebral Palsy
application as a treatment for brain injuries, and the question of its applicationto developmental disabilities including cerebral palsy and rett syndrome.
http://hbot.freeservers.com/

Extractions: and the second Symposium on Cerebral Palsy and the Brain Injured Child (July 25-28, 2001) In Spring 1999, I wrote an extensive literature review paper on hyperbaric oxygen therapy (HBOT) , its demonstrated application as a treatment for brain injuries , and the question of its application to developmental disabilities including cerebral palsy and Rett Syndrome . The paper includes a large number of Internet links and almost 100 scientific references. The goal of the paper is to clearly synthesize important HBOT information that has not previously been presented in one place: on HBOT, the research showing its effectiveness for brain injury, the rationale for its applicability to additional neurological conditions, HBOT treatment protocols, and the data on each of its purported side effects (seen only at high pressures). As of July 2000 this paper is no longer fully current, but I hope to be able to revise it at some point. For now, the many Internet links and references in the paper will lead you to more current information. In particular, see the new 3rd edition of the "Textbook of Hyperbaric Medicine" by K. K. Jain ( click here to view publisher information).
Scientists Create First Animal Model Of Rett Syndrome
MIT. WEDNESDAY, MARCH 21, 2001. Scientists create first animal modelof rett syndrome. By Nadia Halim Whitehead Institute. Researchers
http://web.mit.edu/newsoffice/tt/2001/mar21/rett.html

Extractions: Whitehead Institute Researchers from the Whitehead Institute for Biomedical Research have created the long-awaited animal model for Rett syndrome, one of the most common causes of mental retardation in females with an incidence of one in 10,000-15,000. The transgenic mouse model sheds much-needed light on the underlying mechanism of the disease and suggests a new reason for hope in the research toward therapies. Rett syndrome, caused by a defective gene on the X-chromosome, is thought to have a lethal effect in males before birth or shortly after. Girls with Rett syndrome (and two copies of the X chromosome) are healthy babies who develop normally until six to eighteen months old. But then something goes terribly wrong their health deteriorates and they begin to show symptoms such as loss of speech, loss of voluntary motor control, constant hand wringing and seizures. The work, published in the March issue of Nature Genetics by MIT Professor of Biology
Rett Syndrome & Me
skills. I have classic rett syndrome. Yet it answered so many of their questionstoo. cards. We who have rett syndrome absolutely love music.
http://members.aol.com/Danigirl1/

Extractions: RS is most often misdiagnosed as autism, cerebral palsy or nonspecific developmental delay. While many health professionals may not be familiar with RS, it is a relatively frequent cause of neurological dysfunction in females. The prevalence rate in various countries is from 1:10,000 to 1:23,000 live female births.
Rett Syndrome
Vol. 2, Article 1, Moritani, et al. rett syndrome rett syndrome is a neurodegenerative spasticgait for ten years. Clinically uspected rett syndrome.
http://foundation.asnr.org/neurographics/2/1/1/14.asp

Extractions: Vol. 2, Article 1 Moritani, et al. Rett syndrome Rett syndrome is a neurodegenerative disease of unknown etiology that begins early childhood with autism-like behavior and loss of language skills, and progresses with deterioration of the motor system. Autopsy reveals global hypoplasia in both gray and white matter, which suggests developmental arrest. Increased glutamate in the CSF is reported . MRI shows cerebral hypoplasia, especially in the frontal lobes, and cerebellar atrophy (Figure 14) . MRS shows increased choline and decreased NAA. Increased glucose uptake on FDG PET scans and increased glutamate in the CSF suggest that an excitotoxic mechanism plays an important role in Rett syndrome Figure 14. A 24-year-old female who has a history of autism, seizures and progression of spastic gait for ten years. Clinically uspected Rett syndrome. A. T2WI shows cerebral hypoplasia, especially in bilateral frontal lobes, and secondary skull thickening. B. Sagittal T1WI also shows a thin corpus callosum related to cerebral hypoplasia and skull thickening. Cerebellar atrophy is not prominent in this case.
Rett Syndrome
rett syndrome within the Autism Spectrum, affects only girls and isa unique disorder. rett syndrome Guide picks. rett syndrome is
http://autism.about.com/cs/rettsyndrome/

Extractions: Researchers at Baylor University in Houston, Texas, have identified the gene responsible for Rett Syndrome. This discovery answers a lot of questions and asks even more. One thing we know for sure, is that research dollars are working the way they are intended to work. International Rett Syndrome Association
A Breakthrough For Rett Syndrome
A Breakthrough For rett syndrome. Dateline 03/29 well. What does thisfinding mean to the family of a rett syndrome child? Let's take
http://autism.about.com/library/weekly/aa032900a.htm

Extractions: Rett Syndrome is one of the group of disorders classified as Pervasive Developmental Disorders (PDD's) and is unique in that it affects females exclusively. On September 30, 1999, Dr. Huda Zoghbi of Baylor University , announced that a research team had, after a 16 year search, discovered the gene responsible for Rett Syndrome. The gene, MeCP2 (pronounced meck-pea-two),is a mutation on the X chromosome, and may have implications to other conditions such as Fragile X Syndrome as well. What does this finding mean to the family of a Rett Syndrome child? Let's take a look at some of the implications of this discovery and try to find some answers. First of all, since it is now known that Rett Syndrome does have a genetic cause, it may be possible to develop genetic tests to determine if siblings of Rett patients are asymptomatic carriers. Imagine that a couple knew that one of them was a carrier of this disorder. Would they choose to have children, knowing the risk involved from their own first hand experience? We don't know for sure, but experience with other genetic conditions shows that many parents who carry the gene, choose not to. This could be the case with Rett Syndrome as well. The result of such knowledge could have wide spread impact on not only the incidence of Rett Syndrome, but on the educational, medical and personal decisions a person makes as well.
Special Child: Disorder Zone Archives - Rett Syndrome
rett syndrome Naomi CatfordRobinson. Features and Characteristics. rett syndromeis often mistaken for autism, cerebral palsy, and mental retardation.
http://www.specialchild.com/archives/dz-002.html

Extractions: Rebecca Morris Introduction Rett syndrome (RS) is a genetic disorder that is characterized by an initial period of normal development, followed by a loss of communication skills and purposeful hand movements. It is a disorder that is seen almost exclusively in females and occurs in a variety of racial and ethnic groups worldwide. RS has just recently been traced to a defective gene on the X chromosome called MeCP2. It is estimated that the incidence of RS is between 1 in every 10,000 to 15,000 live female births. Features and Characteristics Rett syndrome is often mistaken for autism, cerebral palsy, and mental retardation. However, no other condition has a period of rapid deterioration followed by stabilization and sometimes even improvements in autistic features, eye contact, and stereotypical hand movements. Since there is no form of laboratory testing for RS, diagnostic criteria and exclusionary criteria have been formed for the recognition of the syndrome. The following characteristics must be found in order to receive a diagnosis of RS: Normal development until approximately 6 to 18 months of age Normal head circumference at birth, followed by a slowed growth rate anywhere from 3 months to 4 years of age
Mississippi Challenge For Rett Syndrome & Leukodystrophy, Beginning May 2003
A World Record Attempt and Film Documentary, The Mississippi River Challengefor rett syndrome And Leukodystrophy Beginning May 10, 2003 -,
http://www.mississippichallenge.org/

Extractions: Clark Eid (Paddler) The Mississippi River Challenge for Rett Syndrome And Leukodystrophy is an ultra-endurance race of the ENTIRE Mississippi River (2,348 miles) without any timeouts or breaks, all done to benefit those suffering from two life threatening diseases - Rett Syndrome and all forms of Leukodystrophy. In May of 2003, Clark Eid (Cheshire, CT) and Bob Bradford (Lapeer, MI) will attempt to paddle the mighty Mississippi River in World Record Time in a specially designed racing canoe. They'll launch their boat and their epic adventure in the still waters of a northern Minnesotan lake and emerge ten states and three weeks later in the Gulf of Mexico. In the days and nights covering 2,348 miles, the two endurance paddlers will race against time, fatigue, foul weather, and unforeseen hazards as they struggle to reach their goal. They are motivated by a love of paddling and the spirit of competition. But behind that, it's a deeply personal undertaking for both men. Clark's daughter has Rett syndrome and Bob's family has been affected by Adrenoleukodystrophy, so they're taking on this unique challenge to raise awareness and research funds to combat these two life threatening diseases.
Mississippi Challenge For Rett Syndrome & Leukodystrophy, Beginning May 2003
The Mississippi River Challenge for rett syndrome And Leukodystrophy Beginning May 10, 2003 -, I'd Like To Support rett syndrome Research!
http://www.mississippichallenge.org/rettsyndrome.html

Extractions: Americans may recognize Rett syndrome as the disorder that Julia Roberts has publicized. Julia Roberts recently spoke about Rett syndrome before Congress in 2002, covered by a well televised CNN news report or from a Rett syndrome documentary she appears in called "Silent Angels" (which appears on the Discovery Health Channel).
-=EZ Medical = - Rett Syndrome -
Ez Figure Logo In Wheelchair Welcome! Your rett syndrome Message Board.Space Coast Early Intervention Center A nationally recognized
http://www.ezeee.org/ezmed/ret.htm
HONselect - Rett Syndrome
English rett syndrome, Autism-Dementia-Ataxia-Loss of Purposeful Hand UseSyndrome - Cerebroatrophic Hyperammonemia - Rett Disorder - Rett's Disorder
http://www.hon.ch/HONselect/RareDiseases/C10.574.500.775.html
Kennedy Krieger Institute Rett Syndrome
Print this page rett syndrome rett syndrome (RS) is a neurological disorder oftenmisdiagnosed as autism, cerebral palsy or nonspecified developmental delay
http://www.kennedykrieger.org/kki/kki_diag.jsp?pid=1101
Kennedy Krieger Institute Rett Syndrome
rett syndrome rett syndrome (RS) is a neurological disorder often misdiagnosedas autism, cerebral palsy or nonspecified developmental delay caused by a
http://www.kennedykrieger.org/accessible/kki_diag.jsp?pid=1101
Rett Syndrome
Researchers on This Project . . . Researchers on All Projects . . .Links to Sites Related to This Project . . . Back to . . . Home
http://www.genetics.ucla.edu/labs/schanen/rett.html
Rett Syndrome Symposium
SLOVENIA. rett syndrome. Organizers Bengt Hagberg (Sweden), AlanPercy (USA) Local organizer Milivoj Velickovic Perat (Slovenia).
http://animus.mf.uni-lj.si/~rett/
Rett Syndrome
rett syndrome up. International rett syndrome Association, The home page forthe International rett syndrome Association. rett syndrome Association UK,
http://omni.ac.uk/browse/mesh/detail/C0035372L0035372.html

Extractions: International Rett Syndrome Association The home page for the International Rett Syndrome Association. The site contains information about Rett (a neurological disorder seen almost exclusively in females), case studies, a discussion group for professionals and the parents of Rett syndrome girls, events, publications, news updates and research contacts. Organizations, Nonprofit Rett Syndrome Rett Syndrome Association UK Rett Syndrome Association UK is a registered charity which offers support to females affected by Rett Syndrome, as well as the carers of these girls and women. Rett Syndrome is a neurological disorder which occurs only in females and those affected are totally dependent on others for their needs. The Rett Syndrome Association UK (RSAUK) provides support for its members in a variety of ways such as, office help, self-support groups, contact supporters network, CarersLine and out of office hours contact numbers. This site provides details about these services, their newsletter, and information about the syndrome. Charities Great Britain Organizations, Nonprofit
Rett Syndrome Research
rett syndrome Research. However, a number of studies have examined boys withrett syndrome, or with the MeCP2 gene defect often found in the syndrome.
http://rarediseases.about.com/library/weekly/aa101202a.htm

Extractions: In 1999 it was discovered that mutations of the MeCP2 (pronounced meck-pea-two) gene were associated with Rett syndrome. A study done in 2002 concluded that the type of mutation corresponded with whether the symptoms of Rett syndrome were mild or severe. Yet other studies could find no clear correlation. Studies show that anywhere from 70% to 80% of cases of the syndrome are caused by the MeCP2 gene defect. Rett syndrome has always been considered to occur only in females, with the thought that the male fetus with Rett syndrome did not survive. However, a number of studies have examined boys with Rett syndrome, or with the MeCP2 gene defect often found in the syndrome. Boys with the MeCP2 gene defect may show different symptoms than "classic" Rett syndrome. Researchers recommend that Rett syndrome remain a clinical diagnosis that should not be dismissed in boys.
Epilepsy Action: Rett Syndrome
rett syndrome. rett syndrome is a condition which occurs in 1 in 1015,000 girls. Girlswith rett syndrome develop normally for the first 6 months of life.
http://www.epilepsy.org.uk/info/rettfrm.html

Extractions: HOMEPAGE EMAIL NEWSLETTER EPILEPSY INFORMATION EPILEPSY ACTION SERVICES ... ONLINE SHOPPING Epilepsy Action is the working name of British Epilepsy Association Rett Syndrome Rett Syndrome is a condition which occurs in 1 in 10-15,000 girls. It does not appear to affect boys. The cause in unknown and it usually does not affect more than one girl in a family. Symptoms Girls with Rett Syndrome develop normally for the first 6 months of life. Between 6 months and 2½ years (often between 6 - 18 months), their development slows up and may even go backwards. They become less interested in play, lose the ability to speak and possibly become irritable. They stop using their hands purposefully and they may, instead, begin to move their hands in a repetitive way, often with hand-wringing movements. Epilepsy is not uncommon, but usually begins after the age of 2 years. The seizures may be of various types including generalised tonic clonic, absences, myoclonic jerks, atonic and tonic. Often, more than one seizure types is present. Frequently, girls with Rett Syndrome have periods of rapid or slow breathing. These periods are sometimes associated with faints, which can be mistaken for epileptic seizures. Diagnosis The diagnosis of Rett Syndrome cannot usually be made with certainty until 3 - 5 years of age. This is because there are specific tests for the condition and the various features are sometimes not present until this age.
Rett (syndrome De)
Translate this page En anglais Rett's syndrome. rett syndrome confirmation of X-linkeddominant inheritance, and localisation of the gene to Xq28.
http://www.vulgaris-medical.com/textr/rett.html

Extractions: Rett (syndrome de) Voir également encéphalopathie, stéréotypie, autisme, microcéphalie. En anglais : Rett's syndrome. Encéphalopathie (atteinte globale de l'encéphale) dont l'origine est inconnue et qui se manifeste entre le 6ème et le 18ème mois chez un enfant de sexe féminin presque exclusivement (la quasi-totalité des malades identifiés sont des filles) qui s'était développé normalement jusque-là. Causes Cette affection a été décrite pour la première fois il y a environ 30 ans par un neuropédiatre de Vienne, Andreas Rett. Ce syndrome, qui au départ été confondu avec l'autisme, a tendance maintenant à être considéré comme un trouble grave et global du développement du système nerveux central. Ce syndrome se transmet génétiquement. En 1999, des anomalies dans le gène Mec P2, sur le chromosome X, ont été mises en évidence chez des filles atteintes du syndrome et également retrouvées chez quelques garçons présentant un handicap sévère. Deux jumelles monozygotes, c'est-à-dire des vraies jumelles issues du même oeuf, seront touchées l'une comme l'autre. Le terme de monozygote est utilisé quand deux jumeaux ont un placenta en commun c'est-à-dire provenant de la division anormale d'un uf fécondé unique au départ.

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