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Triple X Syndrome: Triple X syndrome is a genetic disorder that occurs in women. It is a condition in which a woman has an extra X chromosome in each of her cells, leading to a total of three X chromosomes. This is a rare condition and is usually detected at birth.
What is triple X syndrome?
Normally, women have two X chromosomes. The X chromosomes play a key role in sex determination and control many physical traits. When an extra X chromosome is present, it can affect many organs and systems of the body.
Causes of Triple X Syndrome
Triple X syndrome occurs when the division of chromosomes does not happen correctly during egg and sperm cell formation. This process is called non-disjunction. This is an extremely rare condition that can affect any woman.
Symptoms of Triple X Syndrome
- muscle weakness
- tall stature
- Pain
- Bent fingers
- Delay in language development
- learning difficulties or trouble concentrating
- having a seizure
- wide eyes
- Depression, anxiety, stress
- Kidney, heart, and thyroid problems
- Fertility problems
- Hypothyroidism
- Fatigue and weakness
Treatment of Triple X Syndrome
- Karyotype: This is a test that checks the number and structure of chromosomes.
- FISH test: This is a special test that identifies the spare copy of the X chromosome.
Note: This article provides only general information. Take these only as suggestions. Before acting on any such information, consult a doctor.
