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Fragile X Syndrome Jayce Black March 8, 2011 Abn. Psyc.
Fragile X Syndrome is an inherited condition that affects mostly males because of a change or mutation in the X chromosome formation at time of conception. (From parent to child)
Most individuals = 46 chromosomes;	In females - 2 X’sIn males – X and a YFMR1 – lack of this gene causes Fragile X Syndrome:  ~ this gene produces FMRP (Fragile X Mental Retardation Protein) : ~ which is important in 	brain development:			- Learning	- Behavior 		- Communication
The FMR1gene is given in 3 forms - defined by repeats of a pattern of DNA called CGG repeats: 	~ Individuals with less than 60 CGG repeats = a normal  gene. 	~ Individuals with 60-200 CGG repeats = a 	premutation  (they carry an unstable mutation 	which can expand in future generations.)~ Individuals with over 200 CGG repeats = a	full mutation which causes Fragile X Syndrome. The full mutation causes the gene to shut down = causing the individual to NOTmake FMRP = causing the FMR1 gene to NOT work properly.
Physical characteristics:
Both Diagnosed with Fragile x Syndrome Tyler - 6 Karson - 7
Behavioral characteristics:	~ motor/speech delays	~ hand flapping~ hyperactivity~ impulsive disorderMost children with FXS are very sweet, loving, and have a great sense of humor.
Cognitive deficiencies:~ poor higher-level thinking and reasoning skills ~ difficulty resolving cause and effect questions.Tyler and Karson attending the Marcus Institute in Atlanta in 2007 for 6 months. 	~ Tyler was in the “learning” department.	~ Karson was in the “behavioral” department.
Tyler at the Marcus Institute
Karson at the Marcus Institute
Financial Burdens: ,[object Object]
Tyler – Peachcare/Wellcare
My uncle pays 500 dollars out of pocket every month for Tyler’s medication.

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Fragile x syndrome

  • 1. Fragile X Syndrome Jayce Black March 8, 2011 Abn. Psyc.
  • 2. Fragile X Syndrome is an inherited condition that affects mostly males because of a change or mutation in the X chromosome formation at time of conception. (From parent to child)
  • 3. Most individuals = 46 chromosomes; In females - 2 X’sIn males – X and a YFMR1 – lack of this gene causes Fragile X Syndrome: ~ this gene produces FMRP (Fragile X Mental Retardation Protein) : ~ which is important in brain development: - Learning - Behavior - Communication
  • 4. The FMR1gene is given in 3 forms - defined by repeats of a pattern of DNA called CGG repeats: ~ Individuals with less than 60 CGG repeats = a normal gene. ~ Individuals with 60-200 CGG repeats = a premutation (they carry an unstable mutation which can expand in future generations.)~ Individuals with over 200 CGG repeats = a full mutation which causes Fragile X Syndrome. The full mutation causes the gene to shut down = causing the individual to NOTmake FMRP = causing the FMR1 gene to NOT work properly.
  • 6. Both Diagnosed with Fragile x Syndrome Tyler - 6 Karson - 7
  • 7.
  • 8.
  • 9. Behavioral characteristics: ~ motor/speech delays ~ hand flapping~ hyperactivity~ impulsive disorderMost children with FXS are very sweet, loving, and have a great sense of humor.
  • 10.
  • 11. Cognitive deficiencies:~ poor higher-level thinking and reasoning skills ~ difficulty resolving cause and effect questions.Tyler and Karson attending the Marcus Institute in Atlanta in 2007 for 6 months. ~ Tyler was in the “learning” department. ~ Karson was in the “behavioral” department.
  • 12. Tyler at the Marcus Institute
  • 13.
  • 14. Karson at the Marcus Institute
  • 15.
  • 16.
  • 18. My uncle pays 500 dollars out of pocket every month for Tyler’s medication.
  • 19. The insurance wants Tyler to take the off brand that is cheaper, but the off brand doesn’t help Tyler like the expensive one.
  • 20. treatments are educational interventions designed to increase social skills and to improve intellectual and adaptive functioning. Work with Occupational Therapist and doctors to determine what medications are the best. Treatments
  • 21. Work Cited Schmidt, G. (2010). What is the Cause of Fragile X Syndrome? February 2011. http://www.nfxf.org/html/cause.htm Clapp, K., MS., and Tranfaglia, M. (2010) About Fragile X Syndrome. February 2011. http://www.fraxa.org/aboutFX.aspx Hall, S. S. (2009). Treatments for fragile X syndrome: A closer look at the data. Developmental Disabilities Research Reviews, 15(4), 353-360. doi:10.1002/ddrr.78 Abrams, L. (2010). Summary of Fragile X Syndrome. February 2011.http://www.nfxf.org/html/summary.htm