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Fragile X Syndrome: more books (85)

Spelling Love with an X: A Mother, a Son, and the Gene That Binds Them by Clare Dunsford, 2007-09-04
Alpha-thalassemia X-linked mental retardation syndrome: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Mary, MS, CGC Freivogel, 2005
X-linked mental retardation: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Chitra, MBBS, MD Venkatasubramanian, 2005
Renpenning syndrome: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Charles, PhD Schwartz, 2005
FG syndrome: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Dawn, MS, CGC Jacob, 2005
Smith-Fineman-Myers syndrome: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Judy, MS Hawkins, 2005
FMR1 premutation linked with ovarian failure.(Women's Health): An article from: Internal Medicine News by Mary Ellen Schneider, 2007-08-15
Premature ovarian failure.(GENETICS IN YOUR PRACTICE)(Clinical report): An article from: Internal Medicine News by Howard P. Levy, 2009-10-01
A Doctor's Guide to Weight Control
Options given for ADHD treatment: diagnosable causes.(Children's Health)(Attention Deficit Hyperactivity Disorder): An article from: Family Practice News by Ben Van Houten, 2004-03-01
Chromosomal abnormalities: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Michelle, MS, CGC Bosworth, 2005
Say it with pictures by Marta Lynn Campbell, 1997
X-Linked Mental Retardation 3
Autism:Beyond the Basics by William Shaw Ph.D., Kurt Woeller D.O., et all 2010-05-04

lists with details

CHDD Center - Fragile X Syndrome REA
fragile x syndrome is an inherited disorder with symptoms of mild to severe mental The Research Empahsis Area on fragile x syndrome involves numerous
http://depts.washington.edu/chdd/MRDDRC/REAs/FragileXREA.html

Extractions: Coordinator: Charles Laird, PhD Fragile X syndrome is an inherited disorder with symptoms of mild to severe mental retardation. A wide range of altered cell and molecular phenotypes is caused by an expansion of a triplet repeat in a single gene, FMR1. New and deeper analyses of molecular and clinical data have revealed a greater diversity of clinical and molecular phenotypes in fragile X than was previously evident. The near-completion of the Human Genome Project is yielding new opportunities for molecular discovery and clinical intervention. Moreover, new technologies, such as the chip-based microarray method for sequence analysis, permit systematic molecular characterizations that were previously not feasible. The availability of these new technologies provides a stimulus and focus for our long-term goals: to understand the molecular mechanisms that lead to the fragile X syndrome, how these altered mechanisms lead to clinical symptoms, and how clinical interventions are useful for fragile X patients and their families. The Research Empahsis Area on Fragile X Syndrome involves numerous research groups, some of which are involved in multi-site collaborations.
Mosaïques Association Des "X Fragile"
syndrome de l'X fragile, maladie g©n©tique h©r©ditaire rare avec retard mental, troubles du langage, du comportement, anomalies physiques.
http://perso.wanadoo.fr/mosaiques-xfragile/
Brain Solutions - The Developmental Re-education Centre
Trains parents in multisensory stimulation therapy for children with intellectual and physical disabilities including Down syndrome, fragile X, Rubinstein Taybi, autism spectrum disorders, cerebral palsy, and other kinds of brain injury or damage.
http://brainsolutions.webdynamit.net/
NACD :: The National Association For Child Development
The National Academy for Child Development, Inc. is an international organization of parents and professionals dedicated to helping children and adults reach their full potential. The over 15,000 clients served by NACD have come to us with labels including Learning Disabled, Dyslexic, Distractible, ADD, ADHD, Hyperactive, Down syndrome, Fetal Alcohol syndrome, Williams syndrome, Tourettes syndrome, Rett syndrome, fragile X, Developmentally Delayed, PDD, Autistic, Cerebral Palsy, Brain Injured, Comatose, Retarded, Minimal Brain Dysfunction, Normal, Accelerated and Gifted.
http://www.nacd.org
Allenvale School For Children With Special Needs
Wide range of programmes for children with Autism,Â Prada Willi syndrome, Down's syndrome, fragile X, and Attention Deficit Disorder. Information on the Rainbow Room, multi sensory environment, preschool, main school, young adults, special needs and kids links, school history and vacancies.
http://www.chch.school.nz/allenvale/
Association X-fragile / Index
Explication sur cette maladie qui repr©sente la cause la plus fr©quente de retard mental mod©r© apr¨s la trisomie 21. Projets en cours, agenda des manifestations et publications. Theux.
http://www.x-fragile.be
Ladders.ORG : Learning & Developmental Disabilities Evaluation & Rehabilitation
Dedicated to Research in Autism, Pervasive Developmental Disorder (PDD), Asperger's syndrome, Rett's syndrome, fragile X and Other Developmental Brain Disorders.
http://www.ladders.org/autism.php
Fragile-X Syndrome
links to national and international support groups, clinics with genetic counselors and geneticists.
http://www.kumc.edu/gec/support/fragilex.html

Extractions: 800-688-8765 or 510-763-6030 Fax 510-763-6223 E-mail: natlfx@sprintmail.com Web site: http://www.nfxf.org or http://fragilex.org/ Fragile X Research Foundation of Canada (Fondation Canadienne de Rescherche sur le Syndrome de Fragilite' du Chromosome X), English, French, and Portuguese (including links to other organizations National organizations information on genetic conditions or birth defects Fragile X Syndrome: Diagnostic and Carrier Testing , when and how to test for fragile-X syndrome Policy Statement, American College of Medical Genetics Fragile X , Society for Neuroscience Brain Briefings, 1998 Fragile X Association of Germany (Online der Interessengemeinschaft Fragiles-X e.V.)
Genewatch: Screening For Fragile-X Syndrome [Aug 1997; 42-4]
A monthly newsletter about evidencebased health care; top source for such information on the net.
http://www.jr2.ox.ac.uk/bandolier/band42/b42-4.html

Extractions: @import "../styles/advanced.css"; Skip navigation A recently published report commissioned by the HTA programme sets out the current state of knowledge about screening for the fragile-X syndrome. The work reported involved a comprehensive systematic review of over 500 papers on the subject. Its stated purpose was to provide the information needed to decide whether to use DNA testing to screen for the disorder. In this it is, not surprisingly, only partly successful. Most of its recommendations are for further studies because current information isn't adequate to allow rational decisions to be made about future screening strategies. Fragile-X syndrome is the second most common cause of severe mental retardation after Down's syndrome. The latest population prevalence figures are about 1 in 4,000 for males and 1 in 8,000 for females. About 6% of institutionalised individuals with learning difficulties have the syndrome. It was first described in 1969 and the responsible gene, FMR-1, was identified in 1991. In addition to varying degrees of mental retardation the clinical phenotype often includes macro-orchidism in males, abnormal facies with prominent forehead, large jaw and large ears, joint laxity and behavioural problems. The syndrome gets its name from the fact that chromosomal analysis usually reveals a narrowing near the end of the long arm of the X chromosome (Xq27).
Fragile-X-syndrome Research
? The fragileX-syndrome is the most common hereditary form of mental retardation and occurs much more often in boys than in girls.
http://www.news-medical.net/?id=11179
Introduction: Fragile-X Syndrome - WrongDiagnosis.com
Introduction to fragileX syndrome as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.
http://www.wrongdiagnosis.com/f/fragile_x_syndrome/intro.htm

Extractions: Researching symptoms of Fragile-X Syndrome: Further information about the symptoms of Fragile-X Syndrome is available including a list of symptoms of Fragile-X Syndrome , or alternatively return to research other symptoms in the symptom center Statistics and Fragile-X Syndrome: Various sources and calculations are available in statistics about Fragile-X Syndrome prevalence and incidence statistics for Fragile-X Syndrome , and you can also research other medical statistics in our statistics center
GeneReviews: FMR1-Related Disorders
http://www.geneclinics.org/profiles/fragilex/
Redirectpage
http://www.nfxf.org/home.htm
Www.aap.org/policy/01493.html
http://www.aap.org/policy/01493.html
GeneReviews: FMR1-Related Disorders
http://www.genetests.org/query?dz=fragilex

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