Karyotype 47, XXX
What is it?
Triple X syndrome, or trisomy X, is a genetic disorder affecting women which instead of having only two copies of the X chromosome, have three of it.
Most of the women who have the syndrome do not experience any symptoms while the minority may suffer from developmental delay, seizures or kidney problems.
8 Alikes with Karyotype 47, XXX
Learn from others
who are experiencing
Karyotype 47, XXX.
Additional names
This group contains additional names:
- Triple X Syndrome
Signs & symptoms
Symptoms vary and may include being tall, intellectual disabilities, behavioral problems, developmental delay, learning disabilities, vertical epicanthal folds, widely spaced eyes, flat feet, hypotonia, seizures, kidney problems and premature ovarian failure.
Diagnosis
Diagnosis is based upon findings from medical history and physical examination. Further evaluation may include genetic testing.
Treatment
The syndrome itself has no cure, as there is no way to change the number of chromosomes. Treatment depends on the individual symptoms and needs of each patient.
☝️ This is not a substitute for professional medical advice. Please consult with your physician before making any medical decision.
Learn more about our editorial process for content accuracy.
Source of Information - We analyze big data of more than 23 million patients de-identified medical records from the following sources:
.png)
Find people who are
experiencing a similar
medical reality
Free
Alike Wisdom
Instantly get answers to medical questions with our AI, built from the collective wisdom of our community facing similar experiences
You might also like