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A treatment plan for fragile X syndrome is tailored to the patientâ??s specific needs. Common treatments are: special education, speech and language therapy, occupational therapy, and medication.

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Which syndrome is characterized by the XO chromosome abnormality?

Turner syndrome is characterized by an XO chromosome abnormality, where individuals have only one X chromosome instead of the usual two. This condition can lead to various physical and developmental abnormalities, such as short stature, heart defects, and infertility. Treatment may involve hormone therapy and fertility treatment.


Famous people who have triple x syndrome?

There are no famous individuals known to have Triple X syndrome (also called Trisomy X). Triple X syndrome is a genetic condition that affects females where they have an extra X chromosome (XXY) instead of the typical XX combination. It is a relatively rare condition and may often go undiagnosed.


What happens if a female with Turner Syndrome has the X chromosome inactivated?

If a female with Turner Syndrome inactivates the X chromosome that carries the Turner Syndrome genetic material, she may develop a condition called mosaicism. This can result in a less severe presentation of Turner Syndrome symptoms, as some cells in her body will have the typical number of X chromosomes. However, the exact impact can vary widely among individuals.


Which of the following are example(s) of trisomy---Turner Syndrome Down's Syndrome or Klinefelter's Syndrome?

Trisomy means having three copies of a chromosomes. Turner's syndrome is NOT an example of trisomy. Someone with Turner's syndrome has only one X chromosome. Down's syndrome IS an example of trisomy. Someone with Down's syndrome has 3 copies of chromosome 21. Klinefelter's syndrome is a tricky one. On one hand, it would be considered trisomy because they have 3 sex chromosomes. However, they are not all the SAME sex chromosomes. Someone with Klinefelter's has 2 X chromosomes and one Y chromosome.


Dose marfan syndrome have to be on a x chormose?

Marfan syndrome is caused by a mutation in the FBN1 gene, which is located on chromosome 15 and is inherited in an autosomal dominant pattern. It is not linked to the X chromosome. Both males and females can inherit and display symptoms of Marfan syndrome.