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Fragile X Syndrome: more books (85)

Fragile X syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Judith, MS Sims, Nada, MS, CCGC Quercia, 2006
21st Century Ultimate Medical Guide to Fragile X Syndrome (FRAXA) - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-04-16
Fragile X Syndrome: Medical and Educational Approaches Toward Intervention (Informational) by Randi Jenssen Hagerman, 1994-01
Behavior and Development in Fragile X Syndrome (Developmental Clinical Psychology and Psychiatry) by Elisabeth Dykens, Robert M. Hodapp, et all 1993-11-05
Fragile X-linked syndrome: tell carriers of new risks.(Clinical Rounds): An article from: Family Practice News by Debra Wood, 2004-08-01
Fragile X-associated syndrome: should carriers know of new risks?(Clinical Rounds): An article from: Internal Medicine News by Debra Wood, 2004-04-15
Ocular motor indicators of executive dysfunction in fragile X and Turner syndromes [An article from: Brain and Cognition] by A.G. Lasker, M.M.M. Mazzocco, et all 2007-04-01
Issues and Strategies for Educating Children With Fragile X Syndrome by Philip Wilson, 1994-05
Fragile: Handle with care : understanding fragile X syndrome by Marcia L Braden, 2000
Overview of the Fragile X syndrome: History, diagnosis, etiology, characteristics, and intervention by Donna M Swenson, 1992
Fragile X syndrome: A common cause of mental retardation by Merlin G Butler, 1996
Fragile X syndrome: A handbook for families and educators by Brenda Finucane, 1988
Fragile X Syndrome by Suzanne Saunders, 2000-01-01
Fragile X syndrome: A handbook for families and professionals by Brenda Finucane, 1993

lists with details

Index
In the meantime here is information about fragile x syndrome and The Fragile X Society. fragile x syndrome. What causes Fragile X ? Fragile X Families.
http://www.fragilex.org.uk/

Extractions: Welcome to The Fragile X Society At the moment our Home Page is still under construction. In the meantime here is information about Fragile X Syndrome and The Fragile X Society. Fragile X Syndrome What causes Fragile X ? Fragile X Families The Fragile X Society For more information please contact Email info@fragilex.org.uk Write to: The Fragile X Society, Rood End House, 6 Stortford Road, Great Dunmow, Essex, CM6 1H7 Telephone: The Fragile X Society is a UK registered charity number 1003981.
Fragile X Syndrome
fragile x syndrome. chromosomal abnormality affects males females (1/1000 births); mild familial mental retardation. findings normal
http://chorus.rad.mcw.edu/doc/02033.html
Fragile X Syndrome
fragile x syndrome (aka MartinBell Syndrome, FRAX) is an X-linked syndrome of mental reatrdation associated in a proportion of cases with dysmorphic features
http://www.cmgs.org/BPG/Guidelines/2nd_ed/fragile_x_syndrome.htm

Extractions: Workshops 1992, 1996 Guidelines prepared by David Barton . First draft of this edition, 1 May 1998 IMPORTANT NOTICE: THESE GUIDELINES ARE AT A DRAFT STAGE. THEY ARE POSTED HERE FOR COMMENTS, CORRECTIONS AND AMENDMENTS, AND SHOULD NOT BE USED TO GUIDE LABORATORY PRACTICE UNTIL FORMALLY PUBLISHED. Locus FRAXA Gene FMR-1 OMIM # GeneCard Fragile X Fragile X syndrome (a.k.a. Martin-Bell Syndrome, FRAX) is an X-linked syndrome of mental reatrdation associated in a proportion of cases with dysmorphic features including large everted ears, coarse facies, elongated face and macro-orchidism. Behavioural disturbances including hyperactivity or autistic-like behaviour may be present. Females can also be affected. Approximately one third of female carriers of full mutations will have mild to moderate mental retardation. Most recent publications on the prevalance of FRAX estimate that the disease affects approximately 1 in 5,000 males. 3. THE GENE
Fragile X Syndrome
fragile x syndrome is caused in the vast majority of cases by expansions at a (CGG)n repeat sequence in the promoter region of the FMR1 gene 1-3 . Expansion
http://www.cmgs.org/BPG/Guidelines/1st_ed/fx.htm

Extractions: Workshops 1992, 1996 Guidelines prepared by David Barton Fragile X syndrome is caused in the vast majority of cases by expansions at a (CGG)n repeat sequence in the promoter region of the FMR-1 gene . Expansion of the array above about 200 repeats, accompanied by methylation of the adjacent CpG island, extinguishes expression of the gene. Deletions and point mutations in the FMR-1 coding sequence have also been reported to cause the syndrome . CGG repeat alleles in the 55-200 range are unstable at meiosis and are referred to as premutations. The basis of the most commonly used diagnostic test is sizing of the repeat array by Southern blotting. This is often combined with methylation analysis by restriction enzyme digestion with a methylation-sensitive enzyme. The term "Fragile X syndrome" is commonly used to refer to the syndrome caused by (CGG)n expansions and other lesions in the FMR-1 gene - the FRAXA locus. However, it is now clear that a small number of families which would cytogenetically have been classed as Fragile X have expansions at the nearby FRAXE locus, which also contains an unstable (CGG)n repeat . This repeat can be analysed by PCR as described below. The most commonly used enzymes are EcoRI and HindIII, which give normal fragments of approximately 5.1kb. Several equivalent probes are used, particularly Ox1.913 and StB12.314.
InteliHealth: Fragile X Syndrome
referenced in an AZ format. fragile x syndrome. Health A to Z, Reviewed by the Faculty of Harvard Medical School fragile x syndrome
http://www.intelihealth.com/IH/ihtIH/WSIHW000/9339/9603.html

Extractions: Fragile X Syndrome What Is It? Symptoms Diagnosis Expected Duration ... Additional Info What Is It? Fragile X syndrome is an inherited disorder associated with mental retardation and a particular appearance. It results from an error in a small piece of the DNA (genetic blueprint) for the FMR-1 gene. This gene is found on the X chromosome, one of the two chromosomes, X and Y, that determine gender.
InteliHealth: InteliHealth Home
Health News, Reviewed by the Faculty of Harvard Medical School fragile x syndrome What Is It? fragile x syndrome is an inherited
http://www.intelihealth.com/IH/ihtIH?d=dmtContent&c=210337&p=~br,IHW|~st,333|~r,
Fragile X Syndrome.
fragile x syndrome. (MatinBell Syndrome). Disease Aetiology. In fragile x syndrome, a region of the chromosome has a series of repeats. When
http://www.diseasedir.org.uk/genetic/genex03.htm

Extractions: Chromosomes: X Chromosome Aetiology In fragile X syndrome, a region of the chromosome has a series of repeats. When polymerase begins to replicate the chromosome, polymerase can slip on these repeats, and accidentally enlarges these repeats. In the case of fragile X syndrome, it is thought that when the number of repeats is greater than 200 the gene becomes methylated (a methyl group is added onto the DNA backbone). This methylation causes the gene to become inactive (the promoter becomes inactive, the gene is no longer transcribed). Polymerase is thought to slip when producing the Okazaki fragments during DNA replication. Polymerase can only work in one direction. DNA is said to be asymmetrical, one strand runs in one direction, the other strand runs in the other direction. Polymerase can replicate along one direction uninterrupted, but in the opposite direction polymerase can only move a certain distance before it bumps into itself (see diagram). When polymerase replicates over a large number of repeats, when working in the wrong direction polymerase slips and accidentally copies more of the repeats than there actually are. Later the new repeats become integrated into the chromosome, causing the gene to become inactive once the repeats pass a certain threshold (greater than 200).
EMedicine - Fragile X Syndrome : Article By Jennifer Jewell, MD
fragile x syndrome fragile x syndrome, also termed Martin-Bell syndrome or marker X syndrome, is the most common cause of inherited mental retardation and
http://www.emedicine.com/PED/topic800.htm

Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Last Updated: May 26, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: marker X syndrome, Martin-Bell syndrome, retardation, mental retardation, mental deficiency, FRAXA, X-linked mental retardation AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Jennifer Jewell, MD , Clinical Assistant Professor, Department of Pediatrics, University of Vermont School of Medicine, Pediatric Hospitalist, Barbara Bush Children's Hospital at Maine Medical Center Jennifer Jewell, MD, is a member of the following medical societies: American Academy of Pediatrics American Medical Association Massachusetts Medical Society , and Sigma Xi Editor(s): Michael Fasullo, PhD
Hospital Practice Fragile X Syndrome
Trinucleotide Repetition and fragile x syndrome STEPHEN T. WARREN Emory University. Clinically, fragile x syndrome is hard to recognize, especially in newborns.
http://www.hosppract.com/genetics/9704gen.htm
FRAGILE X SYNDROME : Contact A Family - For Families With Disabled Children: Inf
printer friendly, fragile x syndrome, in affected individuals. 1030 per cent of people with fragile x syndrome develop epilepsy.
http://www.cafamily.org.uk/Direct/f33.html

Extractions: helpful? yes no Fragile X is the most common identifiable form of inherited learning disability . It has a prevalence of about 1 in 4,000 males and 1 in 8,000 females. The cause is an abnormality just above the tip of the X chromosome's long arm, which may be passed from one generation to the next. Intellectual disability varies from mild to severe. Girls and women who have a fragile X chromosome are often of normal intelligence. However up to a third have learning problems which are usually mild or moderate but can occasionally be severe. Other problems experienced by affected individuals include delayed and distorted speech and language development. There can be difficulties with the social use of language, with continuing speech anomalies, repetitive behaviour, attention deficits and overactivity, and autistic-like features, such as poor eye contact, hand flapping, social anxiety, abnormal shyness and an insistence on routine. Physical features ascribed to fragile X syndrome include a relatively large head, a long face with prominent ears, largish jaw and double-jointedness. However these are rarely obvious in affected individuals. 10-30 per cent of people with fragile X syndrome develop
UAB Health System | Fragile X Syndrome
Mansfield. fragile x syndrome. Dear Doctor Column, April 12, 2004. fragile x syndrome Has Wide Range of Symptoms. Question My
http://www.health.uab.edu/show.asp?durki=66712&site=734&return=18687
UAB Health System | Fragile X Syndrome
Stanton. fragile x syndrome. Dear Doctor Column, April 12, 2004. fragile x syndrome Has Wide Range of Symptoms. Question My
http://www.health.uab.edu/show.asp?durki=66712
Fragile X Syndrome - Information / Diagnosis / Treatment / Prevention
home genetic disorders fragile x syndrome fragile x syndrome. Information Fragile X Fact s Page Describing fragile x syndrome. ? Fragile
http://www.healthcyclopedia.com/genetic-disorders/fragile-x-syndrome.html
Fragile X Syndrome
An introduction of fragile x syndrome, followed by links to articles, clinical trials and support groups. fragile x syndrome. Fragile
http://genomelink.org/fragile/

Extractions: Fragile X syndrome, one of the most common causes of mental retardation and neuropsychiatric disease in humans, occurs as a result of the production of fragile sites by trinucleotide repeat expansion of at least one gene located on the X chromosome, which results in problems with learning and behaviour. Learning disabilities are often accompanied by delays in speech and communication skills. There are very good tests to determine whether a person has fragile X, which consists of DNA studies of a blood sample. Acne Allergy Antibiotics Antioxidants ... Wedding Useful Links (Articles, Databases, Support Groups) Neurobiology and Genetics of Fragile X Syndrome - by NIH Guide. Fragile X Syndrome Research - from the Stanford University School of Medicine. Fragile X Syndrome - from the ERIC Clearinghouse on Disabilities and Gifted Education. Research Background- Fragile X - by the University of New South Wales, Faculty of Medicine, School of Anatomy. Fragile X mental retardation - autosomal homolog 2. Fragile X Syndrome - from Public Health Genetics Unit, Cambridge UK.
Fragile X Syndrome
fragile x syndromefragile x syndrome. Affected Males Mental retardation; Long, thin faces prominent jaw; Large, protuberant ears; Macroorchidism; Austistic
http://ibis-birthdefects.org/start/frafact.htm

Extractions: GeneClinics by J Tarleton and RA Saul. " ... characterized by moderate mental retardation in affected males and mild mental retardation in affected females ... all mothers of a child with an FMR1 gene full mutation (expansions >230 trinucletide repeats) are known to be carries of an FMR1 gene expandsion. They and their family members are at increased risk to have children with fragile X syndrome and should be offered DNA-based testing and recurrence risk counseling based on the results. This counseling is extremely complex and should be provided by a knowledgeable genetic professional. Prenatal testing is possible though analysis ... should only be undertaken after carrier status has been ... (1998)."
Pediatric Advisor 2003.2: Fragile X Syndrome
Index. fragile x syndrome. What is fragile x syndrome? fragile x syndrome is an inherited disorder. It is the full mutation that causes fragile x syndrome.
http://www.med.umich.edu/1libr/pa/pa_fragilex_hhg.htm

Extractions: This information is approved and/or reviewed by U-M Health System providers but it is not a tool for self-diagnosis or a substitute for medical treatment. You should speak to your physician or make an appointment to be seen if you have questions or concerns about this information or your medical condition. Index Fragile X syndrome is an inherited disorder. It can cause hyperactivity, learning problems, and emotional problems. It can also cause mental retardation and autism, although some children with fragile X have normal IQs. This disorder is the most common known cause of inherited mental retardation and affects both males and females. Fragile X syndrome is a genetic disorder caused by a mutation (a change in the genetic information) of a specific gene. The parents or other family members did not do anything to cause it. The gene mutation has usually been carried unknowingly for many generations. Both males and female carriers can have a small fragile X mutation (called a premutation) and still be completely normal. The premutation can expand to a larger full mutation when it is passed on to the next generation through a female. It is the full mutation that causes fragile X syndrome. Your child may be the first one in your family with behavior or development problems, or there may be other relatives who are affected by the fragile X mutation. Your doctor or a genetic counselor will explain how this gene mutation is passed on in your family and who should be tested for it.
UMHS Your Child Fragile X Syndrome
Take our online survey. Type in a topic and hit the go button. fragile x syndrome. What is fragile x syndrome? What causes fragile x syndrome? It is inherited.
http://www.med.umich.edu/1libr/yourchild/fragilex.htm

Extractions: Fragile X Syndrome What is Fragile X syndrome? Fragile X is the most common inherited form of mental retardation. It affects about 1 in 1200 males of all racial and ethnic groups. It can cause a range of mental impairment varying from mild to severe , and can also cause many other typical features and symptoms. Here is some basic information about Fragile X. To learn more about genetics and to better understand how genes cause syndromes, see Your Child: Genetic Syndromes It is inherited. It is caused by mutation of a gene ( ) on the X-chromosome. Genetic testing for Fragile X is possible. Mothers may be a carrier of the mutation and pass it on to their children.
What Is Fragile X Syndrome?
fragile x syndrome is second only to Down Syndrome in causing congenital mental retardation and is the leading cause of inherited mental retardation.
http://www.ikm.jmu.edu/Buttsjl/ISAT493/Fragile X Syndrome/fragilexintro.html

Extractions: Main X-linked page Symptoms Incidence Severity ... Prognosis Fragile X Syndrome is second only to Down Syndrome in causing congenital mental retardation and is the leading cause of inherited mental retardation. The disease is diagnosed by Polymerase Chain Reaction (PCR) on the X-chromosome(s) of affected individuals for a fragile area and the FMR1 gene. This fragile area generally results from a lack of folate, which causes triplet repeats in the fragile area of the X chromosome. The more triplet repeats there are on the X chromosome, the more severely affected the individual will be. An individual with less than 50 repeats generally will not be noticeably affected, while an individual with more than 200 repeats will be profoundly affected. In addition, anticipation is seen in the incidence of fragile X syndrome. Anticipation causes the disease to be more severe with each generation that is strikes. Click above to listen to a pronunciation of the disease. When prompted, click 'open from current location'! The figure shown above is the x chromosome. The circled area shows the elongated, decondensed region at the tip of the long arm. This is the "fragile area." This picture was borrowed from
The Neurobiology Of Mental Retardation: Fragile X Syndrome
The Neurobiology of Mental Retardation fragile x syndrome. Deborah Silvis. In my One such disease is fragile x syndrome. Fragile X
http://serendip.brynmawr.edu/bb/neuro/neuro99/web2/Silvis.html

Extractions: On Serendip In my previous paper, I wrote on the topic of the nature-nurture debate and the ways it related to the brain-equals-behavior dilemma. In this paper, I will continue this investigation into the link between genes and neurobiology, but I will focus in on a particular aspect of the relationship: neurological disease caused by genetic aberration. There are many well studied and well documented (thought not necessarily well understood) disorders associated with the X chromosome, and a large number of these have neurobiological roots and behavioral manifestations. One such disease is fragile X syndrome. Fragile X syndrome is the most common inherited form of learning disabilities and mental retardation known . The disease shows an x-linked inheritance pattern and is characterized by a host of symptoms ranging from impaired learning abilities to severe retardation and autistic behaviors . An understanding of the disease is vital on several levels. Fragile X syndrome (FXS) not only bears scientific significance for the fields of molecular genetics, transmission genetics, neurophysiology, and abnormal psychology. It also provides one with a vantage point from which to view the particular set of behaviors known as mental retardation as well as those afflicted by retardation who are too often stigmatized and marginalized in our society.
Inclusive Technology - Fragile X Syndrome
fragile x syndrome. What is Fragile X? fragile x syndrome is the most common inherited cause of learning disability (mental handicap).
http://www.inclusive.co.uk/support/fragilex.shtml

Extractions: home catalogue search downloads ... support organisations The following information is provided by The Fragile X Society. Fragile X Syndrome is the most common inherited cause of learning disability (mental handicap). It occurs more in boys than in girls and is associated with varying degrees of learning difficulty. Boys who are affected almost always have some learning difficulty ranging from mild learning difficulties to severe handicap. Girls are often of normal intelligence but up to a third have learning problems which may be mild or moderated but are occasionally severe. The behaviour features include short attention span, distractibility, impulsiveness and overactivity. Shyness and social withdrawal are often seen in girls who may have difficulties in making friends. Many show autistic-like features - a dislike of eye contact, difficulty in relating to other people, anxiety in social situations often leading to tantrums, insistence on familiar routines and hand flapping or hand biting. Speech and language is usually delayed with continuing speech difficulties and some children and adults develop epilepsy.

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