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Triple X Syndrome
What is Triple X Syndrome?
Triple X syndrome is characterized by the presence of an additional X chromosome.
Triple X Syndrome
How Common is Triple X Syndrome?
This condition occurs in about 1 to 1,000 newborn girls
Can Triple X Syndrome be inherited?
By Kyerston January, Daisy Pogue, Calista Custard, and Matthew
In most cases no, but the additional X sometimes occurs as a random event during the formation of reproductive cells.
How do girls get Triple X Syndrome
An error in cell division called non-disjunction, can result in a reproductive cell with abnormal number of chromosomes.
What are the symptoms to Triple X Syndrome?
1. Tall Stature.
2. Vertical Skin folds that may cover inner corners of the eyes.
3. Delayed speech development
4. Weak muscle tone
5. Curved pinky fingers
6. Behavior and mental heath problems
7. Premature ovarian failure or ovary abnormalities
8. Constipation or abnormalities pain
What treatment, therapy, and/or adaptations are available?
Mrs Ralston
7th Period
If a girl has Triple X Syndrome, treatment is based on her symptoms.