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         Fragile X Syndrome:     more books (85)
  1. Speech & Language Development & Intervention in Down Syndrome & Fragile X Syndrome (Communication and Language Intervention Series) by Joanne E., Ph.D. Roberts, 2007-11-06
  2. Supporting Children with Fragile X Syndrome by Hull Learning Services, 2004-09-30
  3. Children with Fragile X Syndrome: A Parents' Guide
  4. The Broken Toy: A Story of a Fragile X Syndrome Child by Marilyn Morgan, 2005-04-28
  5. X Stories: The Personal Side of fragile X syndrome
  6. Educating Children with Fragile X Syndrome: A Multi-Professional View
  7. Fragile X Syndrome: Diagnosis, Treatment, and Research (Johns Hopkins Series in Contemporary Medicine and Public Health)
  8. The Source for Fragile X Syndrome by Gail Harris-Schmidt, 2004-01
  9. Fragile X Syndrome: A Guide for Teachers by Suzanne Saunders, 2001-03-16
  10. The 2002 Official Patient's Sourcebook on Fragile X Syndrome
  11. Fragile X Syndrome by Randi Jenssen Hagerman, Pamela McKenzie McBogg, 1983-06
  12. The Official Parent's Sourcebook on Fragile X Syndrome: A Directory for the Internet Age by Icon Health Publications, 2005-01-30
  13. New Research on Fragile X Syndrome
  14. The Fragile X Syndrome (Molecular Medicine)

1. Fragile X Syndrome - Wikipedia, The Free Encyclopedia
http//www.wrongdiagnosis.com/f/fragile_x_syndrome/signs.htm; ^ Dölen G, Osterweil E, Retrieved from http//en.wikipedia.org/wiki/fragile_x_syndrome
http://en.wikipedia.org/wiki/Fragile_X_syndrome
Fragile X syndrome
From Wikipedia, the free encyclopedia
Jump to: navigation search Fragile X syndrome
Location of gene ICD Q ICD OMIM ... MeSH Fragile X syndrome , or Martin-Bell syndrome , is a syndrome of X-linked mental retardation . Boys with the syndrome may have large testicles ( macroorchidism prognathism hypotonia and autism , and a characteristic but variable face with large ears, long face, high-arched palate gynecomastia , and malocclusion . Additional abnormalities may include lordosis , heart defect, pectus excavatum flat feet , shortening of the tubular bones of the hands, and joint laxity. Females who have one fragile chromosome and one normal X chromosome may range from normal to mild manifestations of the fragile X syndrome. The fragile X syndrome has an estimated incidence of 1 in 3600 males and 1 in 4,000–6,000 females. Martin and Bell in 1943, described a pedigree of X-linked mental disability, without considering the macroorchidism. In 1969 Chris and Weesam first sighted an unusual "marker X chromosome" in association with mental disability. In 1970 Frederick Hecht coined the term "fragile site" (Renpenning's syndrome is not synonymous with the syndrome). In Renpennig's syndrome there is no fragile site on the X chromosome. Renpenning's cases had short stature, moderate microcephaly, and neurological disorders.

2. Fragile X Syndrome (FXS) Causes, Signs, Symptoms, And Treatments On MedicineNet.
Feb 14, 2007 Read about Fragile X syndrome (FXS or MartinBell syndrome) causes, signs, symptoms, and treatments. Learn the facts about the most common
http://www.medicinenet.com/fragile_x_syndrome/article.htm

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Fragile X Syndrome

3. Fragile X Syndrome
The Official Parent s Sourcebook on FRAGILE X SYNDROME (FRAXA; Marker X Syndrome; MartinBell Syndrome; X-linked mental retardation; X-linked Mental
http://www.icongrouponline.com/health/Fragile_X_Syndrome.html
ICON Health Publications
Official Health Sourcebooks Search ICON Health Titles: The Official Parent's Sourcebook
on
FRAGILE X SYNDROME

(FRAXA; Marker X Syndrome; Martin-Bell Syndrome; X-linked mental retardation; X-linked Mental Retardation and Macroorchidism) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA)
E B O O K Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on . Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms FRAXA; Marker X Syndrome; Martin-Bell Syndrome; X-linked mental retardation; X-linked Mental Retardation and Macroorchidism Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Fragile X Syndrome: Guidelines Overview What Is Fragile X Syndrome? What Causes Fragile X Syndrome? FMRP Production in Fragile X Syndrome Human Cells 101 How Many People Are Affected by Fragile X Syndrome?

4. Fragile_X_syndrome.html 08_26-fragile_X_syndrome.jpg
A normal human X chromosome (left) contrasted with a fragile X chromosome (right), which is prone to breakage in culture. The syndrome is associated with
http://bio3400.nicerweb.com/Locked/media/ch08/fragile_X_syndrome.html
A normal human X chromosome (left) contrasted with a fragile X chromosome (right), which is prone to breakage in culture. The syndrome is associated with excessive repeats of the trinucleotide sequence CGG in the gene, which inactivates this gene. The gene codes for an RNA-binding protein; absence of this protein presumably affects brain development.

5. Health : Conditions_and_Diseases : Genetic_Disorders : Fragile_X_Syndrome : - No
Options. Directory, Entire Web. Top Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome. Fragile X Syndrome (12)
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Pediatric Oncal

- Information presented about Fragile X Syndrome, including the diagnoses and clinical manifestations.
http://www.pediatriconcall.com/fordoctor/diseasesandcondition/fragile_x.asp
Fragile X Research Foundation of Canada

- Registered charity publishes a newsletter, invites applications for research grant, and explains how to donate or join.
http://www.fragile-x.ca/ Maryland Fragile X Resource Group - A community of families in and around the Washington-Baltimore metro area that have children affected by Fragile X Syndrome. Includes news, upcoming events, and resources. http://www.mdfragilex.org/ The National Fragile X Foundation - Features information about the disease, its treatment, and inheritance. http://www.fragilex.org/ Fragile X Association of Australia - Information on this disease, medical aspects, education, references, contacts and what's new in Australia http://www.fragilex.org.au/

6. Buy Fragile_X_syndrome, Sell Fragile_X_syndrome, Trade Fragile_X_syndrome, Illeg
Buy fragile_x_syndrome, Sell fragile_x_syndrome, Trade fragile_x_syndrome, Illegal fragile_x_syndrome, Banned fragile_x_syndrome,
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7. Fragile X Syndrome
Fragile X Syndrome. What is Fragile X syndrome? Fragile X syndrome is the most common form of inherited mental retardation.
http://www.nichd.nih.gov/health/topics/fragile_x_syndrome.cfm
var gMenuControlID=0; var menus_included = 0; var jsPageAuthorMode = 0; var jsSessionPreviewON = 1; var jsDlgLoader = '/health/topics/loader.cfm'; var jsSiteID = 8; var jsSubSiteID = 21; var kurrentPageID = 7633; document.CS_StaticURL = "http://www.nichd.nih.gov/"; document.CS_DynamicURL = "http://www.nichd.nih.gov/"; changeBanner('/health/topics/'); Last Update: 09/07/2006 Printer Friendly Email This Page Fragile X Syndrome What is Fragile X syndrome? Fragile X syndrome is the most common form of inherited mental retardation. Fragile X happens when there is a change, or mutation, in a single gene called the Fragile X Mental Retardation 1 (FMR1) gene. This gene normally makes a protein the body needs for the brain to develop. But when there is a change in this gene, the body makes only a little bit or none of the protein, which can cause the symptoms of Fragile X. Fragile X is inherited, which means it is passed down from parents to children. Parents can have children with Fragile X even if the parents do not have Fragile X themselves. The changes in the gene can become more serious when passed from parent to child. Some people may only have a small change in their FMR1 gene (called a premutation ) and may not show any signs of Fragile X. Other people may have bigger changes in the gene, called a

8. Il Trovatore Directory Mondo Health Conditions_and_Diseases Genetic_Disorders Fr
Iltrovatore, il tuo amico sulla Rete mail e internet gratis, canali tematici con i migliori siti per ogni argomento e tante pagine e servizi per sfruttare
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9. Health Conditions And Diseases Genetic Disorders Fragile X Syndrome On NYMSD - N
Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome listings in NYMSD National Yellow Multi Services Directory.
http://www.nymsd.com/web/sites.cgi?page=/Health/Conditions_and_Diseases/Genetic_

10. Kamusta - The Pinoy Web Directory - Philippines : Health : Conditions_and_Diseas
Top Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome. Fragile X Syndrome. See Also. Top/Health/Conditions and Diseases/Neurological
http://uk.tagoror.com/index.php/Health/Conditions_and_Diseases/Genetic_Disorders
[ifrss] [ifrss] Save your Bookmarks Suggest a site Search Options: entire directory this category only advanced Top Health Fragile X Syndrome See Also: Sites:
Carolina Fragile X Project
- A series of studies examining the impact of fragile X syndrome (FXS) on individuals, families and the agencies that serve them.
Conquer Fragile X, Inc.
- Creating a virtual research center in Israel to find a cure.
FRAXA Research Foundation Home Page
- Non-profit organization run by parents. Fighting to find a cure for Fragile X Syndrome and helping Fragile X Family's.
Fragile X Association of Australia
- Information on this disease, medical aspects, education, references, contacts and what's new in Australia
Fragile X Association of Southern California
- Fragile X Syndrome is the leading inherited cause of developmental disabilities and mental impairment worldwide. It affects 1 in 2,000 males and 1 in 4,000 females. It is estimated that 1 in 259 females are carries of the premutation.
Fragile X Research Foundation of Canada
- Registered charity publishes a newsletter, invites applications for research grant, and explains how to donate or join.

11. Fragile X Syndrome
Links to information to do with Fragile X Syndrome.
http://www.healthinsite.gov.au/topics/Fragile_X_Syndrome
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Fragile X Syndrome
Fragile X Syndrome is a hereditary condition which causes a wide range of mental impairment, from mild learning disabilities to severe mental retardation. It is also associated with a number of physical and behavioural characteristics. Follow the links below to find information on Fragile X Syndrome. Updated January 2008 Printer friendly page
4 Resources Found
Results 1 to 4 displayed. Title: Chromosome Defects
Publisher: HealthInsite Topic Page
Description: Links to information about chromosome defects, including Down Syndrome and Fragile X Syndrome.
Date: Jan 2008 Title: Fragile X
Publisher: Child and Youth Health - CYH (South Australia)
Description: Fragile X causes problems with learning and behaviour. It is the most common inherited cause of intellectual disability. It is found worldwide, in all races and societies.

12. Fragile-X Syndrome - WrongDiagnosis.com
FragileX Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
http://wrongdiagnosis.com/f/fragile_x_syndrome/intro.htm
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Contents: Fragile-X Syndrome
  • Introduction: Fragile-X Syndrome Full Text Books Online Symptoms Misdiagnosis ... Full Contents list
  • Introduction: Fragile-X Syndrome
    Fragile-X Syndrome: Fragile X syndrome is the most common inherited form of mental retardation currently known. (Source: Genes and Disease by the National Center for Biotechnology) ... more about Fragile-X Syndrome Fragile-X Syndrome: A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females. More detailed information about the symptoms causes , and treatments of Fragile-X Syndrome is available below.

    13. Fragile X Syndrome - Conservapedia
    http//www.genome.gov/glossary.cfm?key=Fragile%20X%20syndrome. Retrieved from http//www.conservapedia.com/fragile_x_syndrome . Category Genetics
    http://www.conservapedia.com/Fragile_X_syndrome
    Fragile X syndrome
    From Conservapedia
    Jump to: navigation search Fragile X syndrome is the second most frequent genetic cause of mental retardation, after Down's syndrome . The disorder is one of a group of diseases that results from an unusual kind of mutation: an expansion of a repeating sequence of three letters of the DNA code, called a triplet repeat or trinucleotide repeat In Fragile X, the repeating triplet is CGG, cytosine-guanine-guanine, in a gene called FMR1 on the X chromosome. There are ordinarily fewer than 55 copies of the repeat. When the number of repeats exceeds 200, the expansion is called a "full mutation" and expression of the FMR1 gene is shut off, causing the fragile X syndrome. Individuals who carry between 55 and 200 copies of the repeat, called a "premutation", may transmit a gene with a full mutation (>200 repeats) to their children, but are generally not affected by the full-blown fragile X syndrome themselves. Carriers of premutations may have difficulties with mild cognitive or behavioral problems, premature ovarian failure in female carriers,and an adult-onset neurological disorder causing tremor and difficulties with balance and gait.
    edit Sources
    http://www.genome.gov/glossary.cfm?key=Fragile%20X%20syndrome

    14. Fragile X Syndrome - Descipher Health
    External Links. Retrieved from http//www.descipher. com/health/info/fragile_x_syndrome . Views. Article; Discussion; Edit; History. Personal tools
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    Fragile X syndrome
    From Descipher Health
    Description: Table of contents showTocToggle("show","hide") 1 Synonyms
    2 Cause

    3 Population Distribution

    4 Effects
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    Martin-Bell syndrome, FRAXA, marker X syndrome edit
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    15. Fragile X Syndrome
    After Down syndrome, the second most frequent genetic cause of mental retardation. The disorder is one of a group of diseases that results from an unusual
    http://www.daviddarling.info/encyclopedia/F/fragile_X_syndrome.html

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    fragile X syndrome
    After Down syndrome, the second most frequent genetic cause of mental retardation. The disorder is one of a group of diseases that results from an unusual kind of mutation : an expansion of a repeating sequence of three letters of the DNA code, called a triplet repeat or trinucleotide repeat.
    In fragile X, the repeating triplet is CGG, cytosine-guanine-guanine, in a gene called FMR1 on the X chromosome . There are ordinarily fewer than 55 copies of the repeat. When the number of repeats exceeds 200, the expansion is called a "full mutation" and expression of the FMR1 gene is shut off, causing the fragile X syndrome.
    Individuals who carry between 55 and 200 copies of the repeat, called a "premutation", may transmit a gene with a full mutation (more than 200 repeats) to their children, but are generally not affected by the full-blown fragile X syndrome themselves.
    Carriers
    of premutations may have difficulties with mild cognitive or behavioral problems, premature ovarian failure in female carriers,and an adult-onset neurological disorder causing tremor and difficulties with balance and gait.
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    HEALTH AND DISEASE

    GENETICS AND HEREDITY
    Source: National Human Genome Research Institute Also on this site: Encyclopedia of History BACK TO TOP var site="s13space1234"

    16. Fragile X Syndrome LinkedWords™ - Contextually Find And Manage Web Inf
    Added April 6, 2006, 233 am Found in page http//www.linkedwords. com/science/anomalies-and-alternative-science/fragile_x_syndrome.php - Main site
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    17. Name Type Website - For More Info Author Fragile X Syndrome
    The Official Parent s Sourcebook on FRAGILE X SYNDROME, book, www.icongrouponline.com/health/fragile_x_syndrome.html, James N and Phillip M Parker Editors
    http://www.fraxa.org/catalog.htm
    Name Type website - for more info Author Fragile X Syndrome: Diagnosis, Treatment, and Research book Randi Jenssen Hagerman, MD Children with Fragile X Syndrome: A Parents' Guide book Jayne Dixon Weber (Editor) Fragile X Syndrome: A Guide for Teachers book Suzanne Saunders Fragile X Fragile Hope: Finding Joy In Parenting A Special Needs Child book Elizabeth Griffin The Broken Toy book www.authorhouse.com/BookStore/ItemDetail.aspx?bookid=28995 Marilyn Morgan, MS Ed. Fragile: Handle with Care book www.fragilex.org Marcia Braden The Source® for Fragile X Syndrome book www.fragilex.org Gail Harris-Schmidt, Ph.D. and Dale Fast, Ph.D. Transitioning "Special" Children Into Elementary School book www.fragilex.org Jayne Dixon Weber Boys with Fragile X Syndrome book www.fragilex.org Rebecca O'Connor, MA My Extra Special Brother book http://www.fraxa.org/aboutFraxa_resources.aspx Carly Heyman Medication Guide for Fragile X book http://www.fraxa.org/aboutFraxa_resources.aspx Michael Tranfaglia MD Fragile X, A to Z

    18. > Health> Conditions And Diseases> Genetic Disorders> Fragile X Syndrome>
    Books on fragile_x_syndrome. Music Music on fragile_x_syndrome. Videos Videos on fragile_x_syndrome. See also. Health Conditions and Diseases
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    19. Fragile X Syndrome - Glasgledius
    Fragile X syndrome. Fragile X Syndrome is the most common cause of mental retardation, affecting approximately 1 in 1500 males and 1 in 3000 females
    http://www.glasglow.com/e2/fr/Fragile_X_syndrome.html
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    Fragile X syndrome
    Fragile X Syndrome is the most common cause of mental retardation , affecting approximately 1 in 1500 males and 1 in 3000 females (figures given vary; these are approximations). It is caused by a mutation of a region of the X chromosome , and specifically, an excessively large number of repetitions of a specific gene on that chromosome. Because men receive only one copy of the X chromosome, most (all?) males with the mutation exhibit at least some symptoms of the syndrome, while only approximately 30 percent of females will exhibit significant symptoms, with the rest being carriers of the mutation. Aside from mental retardation, the most obvious indicators include physical differences and behaviors commonly associated with autism . Of the former, the most readily visible are an elongated face and large or protruding ears, but others are also frequently present. Of the latter, behavioral stereotypy and atypical social development are the most frequently observed. Because the underlying cause is genetic, there is no cure. The syndrome can be treated through behavioral therapy, special education, and where necessary, treatment of physical abnormalities. Persons with Fragile X in their family histories are advised to seek genetic counseling to assess the likelihood of having children who are affected, and how severe any impairments may be in affected descendants.

    20. Fragile X Syndrome - Associated Content
    href= http//www.associatedcontent.com/article/23684/fragile_x_syndrome.html /23684/fragile_x_syndrome.html /a br br Submit your original video,
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    Fragile X Syndrome
    Joanne E. Roberts' Look at the Communication of Young Males with FXS
    By Shari Moore , published Mar 09, 2006 Published Content: 9 Total Views: 3,478 Favorited By: CPs Contact Subscribe Add to Favorites Rating: 3.0 of 5
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    Font Font Fragile X syndrome (FXS) is looked at in a new children and more sever in adolescents and adults. These deficits include those concerning social interaction and pragmatics, semantic and syntactic delays and phonological deficits.
    The research among these deficit areas is difficult to decipher because the data across age groups tends to differ within categories. For instance, adolescent and adult males may have intelligible single word speech and poor conversational speech, but still have preservation within single words. Another piece of data that also illustrates this inconsistency amongst data is that adult males with FXS tend to have a smaller range of grammatical construction whereas children who do not have FXS and are normally developing and perform at the same mental age children younger than 8 with FXS.

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