Fragile X Syndrome By shannon perry

Fragile X Syndrome is particularly common in the USA, 1 in 151 females or 1 million women in the USA. 1 in 250-800 or 320,000 men in the USA are affected by this Syndrome.

Signs/Symptomms: Behaviour - Aggression, hyperactivity, impulsivity, nonsense word repetition, repetitive movements, self-harm. Developmental- Learning disability or speech delay in a child. Muscular- Flaccid muscles or problems with coordination. Also Common- Large ears, speech impairment, enlarged head, flat feet, lazy eyes, long face, prominent jaw, scoliosis, single line on palm, sleep disorders, sunken chest or tremor.

Inheriting this is known as a X-Linked that mutated gene which causes the disorder at the X chromosome, on of the two ( Y is the other sex chromosome) It is dominant if a singular copy of the changed gene in each cell is sufficient to cause the condition.

Location of the gene: The gene is located on the X chromosome, one of the two sex chromosomes.

Pedigree:

Tests: The diagnosis of Fragile X Syndrome can be determined through a DNA blood test. Test results with typically take between between 4-8 weeks typically to determine whether or not a child carries the Syndrome.

Life Expectancy: Male rate 5-25 years, 20% of woman population experience premature ovarian failure which means there mensturaltion period stop at age 40 and is age expectancy.

Quality of Life: Living with Fragile X Syndrome can be challenging in many aspects and determine life quality isn't determinable depending on what life style they live from when there born will determine life quality.

Report Abuse

If you feel that this video content violates the Adobe Terms of Use, you may report this content by filling out this quick form.

To report a Copyright Violation, please follow Section 17 in the Terms of Use.