AD
LEEP INK FEATURES
Part II
There are several unique focuses for 2025. I covered the first 12 in Part One. The following are the rest I have discovered for this year. As with all issues of LEEP Ink, the following descriptions are a...
January—It is a New Year!
We've arrived at another new year; the older I get, the more frequently they come. When I was younger, years seemed to take a long time to pass. Now, they're just a blip—here and gone. For ma...
2025 is the Year of...
21 Themes and 'Year of' Events for 2025 PART ONE, THE FIRST 12 Every year, various organizations announce the theme for the year. These themes can focus on causes, such as aesthetics and color tre...
About Fragile X Awareness Month
Education , Lifestyle
Family & Friends , United States
Ends: Jul 31, 2024
DESCRIPTION:
ABOUT FRAGILE X AWARENESS MONTH
Fragile X Syndrome (FXS) is a genetic disorder that causes intellectual disability, behavioral and learning challenges, and various physical characteristics. It is the most common inherited cause of intellectual disability and autism.
Causes of Fragile X Syndrome
Fragile X Syndrome begins with a mutation in the FMR1 gene located on the X chromosome. This gene produces a protein called FMRP, essential for normal neural development. In individuals with FXS, a section of the FMR1 gene called the CGG triplet repeat is expanded. Symptoms of Fragile X Syndrome
The symptoms of Fragile X Syndrome can vary widely among individuals, but common signs include:
Intellectual and Developmental Delays
Physical Characteristics:
Sensory Sensitivities:
Sensitivity to light, sounds, textures, and other sensory inputsPrevalence of Fragile X Syndrome
Fragile X Syndrome affects both males and females, though males are typically more severely affected due to having only one X chromosome.
In Males: Approximately 1 in 4,000 to 1 in 7,000.
In Females: Approximately 1 in 8,000 to 1 in 11,000.
The variability in these estimates is due to differences in study methodologies and population sampling.
Summary
Fragile X Syndrome is a significant genetic disorder caused by a mutation in the FMR1 gene. It leads to a range of cognitive, behavioral, and physical symptoms. It is relatively rare, affecting a small percentage of the population, with males being more severely affected than females. Early diagnosis and intervention can help manage symptoms and improve the quality of life for individuals with FXS.
VIDEOS
SUPPORTING DOCUMENTS
Currently, this event does not have supporting documents.
ADDITIONAL IMAGES
Currently, this event does not have supporting images.
Where would you like to go now?
AD
/footer-logo.svg){kind=logo}
LEGAL: Excerpts and links may be used, provided that full and clear attribution is given to Jubilee LLC and LEEPCalendar.com, with appropriate and specific direction to the original content (Page URL). Additional documents, embedded videos and additional image rights retained by their creators and are provided to increase understanding of the event or topic.
Jubilee LLC reserves the right to accept or reject inclusion of events in this calendar. The appearance of an event in LEEP Calendar does not imply endorsement of the event, nor the organization championing the event by Jubilee LLC, its stakeholders, customers or subsidiaries. All dates, contact information, URLs, addresses, and information relating to any event, promotion or holiday are subject to change without notice and should be treated as estimated. Jubilee LLC, our stakeholders, customers and subsidiaries cannot warrant accuracy. Users of this application are solely responsible for verifying actual event date with organizers and additional sources prior to committing resources, financial, human or otherwise.
Jubilee LLC, 1712 Pioneer Avenue,Suite 2019 Cheyenne, WY 82001 +1 (484) 226 4777
Copyright © Jubilee LLC / LEEPCalendar.com 2025. All rights reserved.
/Icon awesome-facebook-square.svg)
/Icon awesome-instagram.svg)
/Icon awesome-twitter-square.svg)
/Icon awesome-linkedin.svg)
/Icon awesome-behance-square.svg)