Fragile X syndrome, is a genetic syndrome which results in a spectrum of characteristic physical, intellectual, emotional and behavioral features which include an elongated face, large or protruding ears, flat feet,
Fragile X Syndrome (also known as FXS) is a life-altering condition that causes intellectual frailty. Those affected are prone to behavioral and learning challenges and may have physical imperfections.
Children and adults with fragile X syndrome have a number of mental and physical signs and symptoms ranging from mild to severe. Males tend to be more severely affected than females. Common mental symptoms include:
Individuals with fragile X syndrome may have subtle physical signs that tend to become more obvious with age. These may include:
Girls with fragile X syndrome generally have fewer physical signs of the condition than males. While most males with fragile X syndrome have intellectual disabilities, only about one-third to one-half of affected females do. However, affected girls with normal intelligence may have some of the following symptoms:
The characteristics of Fragile X syndrome include an elongated face, protruding ears, and large testes. Fragile X is the single most common one gene cause of autism.
To have Fragile X syndrome means that someone has a genetic syndrome, the most widespread single-gene cause of autism and inherited caused of autism and mental retardation for boys.
No, fragile x syndrome is not progressive
The fragile X syndrome is a genetic disorder caused by mutation of the FMR1 gene on the X chromosome.
Martin Bell Syndrome.
Early diagnosis and intensive intervention offer the best prognosis for individuals with fragile X syndrome. Adults with fragile X syndrome may benefit from vocational training and may need to live in a supervised setting. Life span is typically normal
also known as Martin-Bell syndrome, Marker X syndrome, and FRAXA syndrome
Martin bell
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"Chromosomal analysis" should not be used for Fragile X Syndrome determination. Chromosomal analysis, Karotyping, has proven unreiable in diagnosis. Detemination can be made through DNA testing for Fragile X Syndrome, FMR1 DNA test.
affects males and females of all ethnic groups. It is estimated that there are about one in 4,000 to one in 6,250 males affected with fragile X syndrome. There are approximately one-half as many females with fragile X syndrome as there are males
mutation
Martin Bell Syndrome.
yes