Group items tagged fragile x - PLUK eNews

Fragile X Associated Disorders, More than a Syndrome - Webinar - Feb. 20, 2013 - 0 views

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webinar fragile X syndrome

shared by Sierra Boehm on 28 Jan 13 - No Cached

Sierra Boehm on 28 Jan 13

Click here to register for this webinar What: This webinar will discuss the spectrum of disorders associated with the FMR1 gene mutation: Fragile X Syndrome (FXS), Fragile X Primary Ovarian Insufficiency (FXPOI), and Fragile X Tremor Ataxia Syndrome (FXTAS). FXS is the leading known cause of autism and the most prevalent inheritable cause of intellectual disabilities. FXPOI affects 15-20% of women who have the premutation allele of the FMR1 gene and involves clinical features including irregular menses, reduced fertility and premature menopause. Also within the premutation range, the neurodegenerative condition known as FXTAS can occur in 46% of males and 17% of women. This webinar will provide a basic understanding of the FMR1 gene mutation, prevalence and clinical features of FX Associated Disorders. A discussion of the varied clinical presentations, associated health conditions and the most recent research on treatments will be included. When: Wednesday, February 20, 2013 12:00 pm - 1:00 pm Mountain Cost:
Free

<div class="cArrow"> </div><div class="cContentInner">Click here to register for this webinar What: This webinar will discuss the spectrum of disorders associated with the FMR1 gene mutation: Fragile X Syndrome (FXS), Fragile X Primary Ovarian Insufficiency (FXPOI), and Fragile X Tremor Ataxia Syndrome (FXTAS). FXS is the leading known cause of autism and the most prevalent inheritable cause of intellectual disabilities. FXPOI affects 15-20% of women who have the premutation allele of the FMR1 gene and involves clinical features including irregular menses, reduced fertility and premature menopause. Also within the premutation range, the neurodegenerative condition known as FXTAS can occur in 46% of males and 17% of women. This webinar will provide a basic understanding of the FMR1 gene mutation, prevalence and clinical features of FX Associated Disorders. A discussion of the varied clinical presentations, associated health conditions and the most recent research on treatments will be included. When: Wednesday, February 20, 2013 12:00 pm - 1:00 pm Mountain Cost:<br />Free</div>

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Drugs Could Hold Key To Unlocking Fragile X - Disability Scoop - 0 views

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fragile x medication

shared by Roger Holt on 02 Mar 10 - Cached

In an effort once considered unimaginable, scientists are testing a series of drugs which they hope will improve the mental abilities of individuals with fragile X syndrome. Unlike currently available drugs that treat symptoms of fragile X — like anxiety — the new medications now in trials are designed to address core components of the disorder. The idea is not to cure fragile X, but rather to improve the mental functioning abilities of those who have it.
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CDC Features - Fragile X Syndrome and Associated Disorders - 0 views

www.cdc.gov/FragileX

CDC fragile x

shared by Roger Holt on 22 Jul 11 - No Cached

Fragile X syndrome and fragile X-associated disorders are a group of genetic conditions that can affect individuals and their families in many ways. Find out more about fragile X syndrome and fragile X-associated disorders.
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12 Important Resources for Families with Fragile X Syndrome | Friendship Circle -- Spec... - 0 views

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fragile x

shared by Roger Holt on 14 Aug 12 - No Cached

Being a parent to a child with a disability, any disability, is like day after day of guiding your family’s boat through a constant storm.  For parents of a child with Fragile X Syndrome, a leading cause of autism and intellectual disabilities, the storm may seem to rage on and on. To help you get though the tough times we have provided a list of 12 must have Fragile X resources.
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NIH To Study Fragile X In Depth - Disability Scoop - 0 views

www.disabilityscoop.com/...4208

study fragile x NIH

shared by Roger Holt on 21 Jul 09 - Cached

Federally funded research into fragile X syndrome will look at the biological factors of the disorder and ways to better diagnose and treat it, according to a research plan released by the National Institutes of Health (NIH) Monday.
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Trials Beginning On Drug To 'Correct Or Improve' Fragile X - Disability Scoop - 0 views

www.disabilityscoop.com/...6004

fragile x medication research

shared by Roger Holt on 03 Nov 09 - Cached

The drug, currently called STX107, targets altered brain connections that appear in individuals with fragile X. Researchers hope that the drug will force the brain to make normal connections therefore improving learning capabilities in those with the disorder.
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PLUK News feed: Children with Fragile X Syndrome and their Families Webinar Archived - 0 views

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Children Family Fragile X Syndrome webinar

shared by Kiona Pearson on 05 Jul 11 - No Cached

Click here to view the webinar What: The Children with Fragile X Syndrome and their Families webinar has been archived and is now available for viewing online.
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Genetic Syndromes: Etiology and Educational Techniques - Billings - Mar. 14, 2013 - 0 views

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education genetic disorders Montana

shared by Sierra Boehm on 01 Mar 13 - No Cached

Sierra Boehm on 01 Mar 13

Click here to download the flier for this event
Click here to register for this event

What:
Marissa Clark, Genetic Counselor at Shodair Hospital, will be presenting on a variety of topics that are commonly seen in genetics clinic as it relates to educational needs and support. The focus of the presentation will primarily be on fetal alcohol syndrome (FAS) and fetal alcohol effects (FAE); however, less common genetic syndromes such as: neurofibromatosis, elhers-danlos syndrome, fragile X, and chromosomal microdeletion/micoduplication disorders will be covered. In addition to the etiology of the genetic syndromes, helpful educational techniques and resources will be addressed, as well as the signs and symptoms that educators should be aware of. There will be ample time for a question and answer session that can address individual cases and situations.

When:
Thursday, March 14, 2013
11:30 am - 1:30 pm Mountain Where:
MSUB College of Education Building, Room 122
MSU-Billings Campus
1500 University Dr.
Billings, MT 59101 Cost:
$15.00 Non refundable - Includes luncheon buffet (Two OPI Renewal Units available)

Contact:
Debra Miller, Region

<div class="cArrow"> </div><div class="cContentInner"> Click here to download the flier for this event<br />Click here to register for this event<br /><br />What:<br />Marissa Clark, Genetic Counselor at Shodair Hospital, will be presenting on a variety of topics that are commonly seen in genetics clinic as it relates to educational needs and support. The focus of the presentation will primarily be on fetal alcohol syndrome (FAS) and fetal alcohol effects (FAE); however, less common genetic syndromes such as: neurofibromatosis, elhers-danlos syndrome, fragile X, and chromosomal microdeletion/micoduplication disorders will be covered. In addition to the etiology of the genetic syndromes, helpful educational techniques and resources will be addressed, as well as the signs and symptoms that educators should be aware of. There will be ample time for a question and answer session that can address individual cases and situations.<br /><br />When:<br />Thursday, March 14, 2013<br />11:30 am - 1:30 pm Mountain Where:<br />MSUB College of Education Building, Room 122<br />MSU-Billings Campus <br />1500 University Dr. <br />Billings, MT 59101 Cost: <br />$15.00 Non refundable - Includes luncheon buffet (Two OPI Renewal Units available)<br /><br />Contact: <br />Debra Miller, Region </div>

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Episode 2: CDC's Life Course Model for Children and Young Adults With Chronic Condition... - 0 views

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CDC Fragile X Syndrome Life Course Model Muscular Dystrophy Spina Bifida Webinar

shared by danny hagfeldt on 21 Nov 11 - No Cached

Reserve your spot here!What:This webinar will focus on CDC's Life Course Model and public health approach for rare and complex disabling conditions, such as fragile X syndrome, muscular dystrophy and spina bifida.  Panelists will provide an overview of childhood-onset conditions, discuss current approaches to data collection, and describe how CDC incorporates a life course approach into its work.When: Tuesday, November 29, 20112:00 PM - 3:00 PM MT
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Q2 KTVQ | Billings | Huntley Project senior an inspiration on the court - 0 views

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Montana fragile x disability sports

shared by Roger Holt on 06 Feb 10 - Cached

Ask most basketball players if they'd mind subbing in to a game with less than a minute to play - they'd *scoff* at the notion.  But not Huntley Project senior Sam Shaules.  Q2's Casey Conlon has the heart-warming story of the 30 seconds of game-time that not only make his night - but his entire season.
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