Trisomy X, also known as Triple X syndrome, is a genetic condition that occurs in 1 in 1,000 girls where they have an extra X chromosome, for a total of three X chromosomes instead of the typical two. It is usually inherited from the mother and risk increases with the mother's age. Those with Trisomy X can experience mild cognitive impairment, developmental delays, learning disabilities, and mood disorders. While there is no cure, early diagnosis and intervention can improve developmental outcomes through medical care and therapy.
Trisomy X, also known as Triple X syndrome, is a genetic condition that occurs in 1 in 1,000 girls where they have an extra X chromosome, for a total of three X chromosomes instead of the typical two. It is usually inherited from the mother and risk increases with the mother's age. Those with Trisomy X can experience mild cognitive impairment, developmental delays, learning disabilities, and mood disorders. While there is no cure, early diagnosis and intervention can improve developmental outcomes through medical care and therapy.
Trisomy X, also known as Triple X syndrome, is a genetic condition that occurs in 1 in 1,000 girls where they have an extra X chromosome, for a total of three X chromosomes instead of the typical two. It is usually inherited from the mother and risk increases with the mother's age. Those with Trisomy X can experience mild cognitive impairment, developmental delays, learning disabilities, and mood disorders. While there is no cure, early diagnosis and intervention can improve developmental outcomes through medical care and therapy.
syndrome or 47, XXX, is a genetic condition that occurs in females? It's not very common, affecting only around 1 in 1,000 girls. But the good news is that it can be managed with proper medical care. If you or someone you know is affected by Trisomy X, know that you're not alone and there are resources available to help you. Trisomy X is a genetic condition that occurs in females when they have an extra X chromosome in all their cells. This leads to a total of three X chromosomes, instead of the typical two. The syndrome is usually inherited from the mother, and the risk of its occurrence increases with the mother's age. This condition occurs only in individuals who were assigned female at birth (AFAB). Physical characteristics Poor muscle tone (hypotonia) Wide-spaced eyes (hypertelorism) Vertical skin folds that cover the inner corners of the eyes (epicanthal folds) Curved or bent little fingers (clinodactyly) Neurological conditions Mild cognitive impairment. Developmental delays Learning disabilities Attention-deficit/hyperactivity disorder. Mood disorders like anxiety and depressionly Other medical conditions Autoimmune conditions Differences in heart structure Frequent urinary tract infections. Genito-urinary deformities or malfunctions Kidney abnormalities There’s no cure for triple X syndrome. However, early diagnosis and intervention can make a big difference in improving developmental outcomes for those affected. So if you or someone you know is facing this challenge, remember that there is hope and support available! After a diagnosis, it is possible that your healthcare provider may order additional tests.
Renal ultrasound to look at the structure of
your kidneys.
Cardiology consultation or EKG/echocardiogram
to evaluate your heart.
Neurology consultation and neuropsychological
testing. Your healthcare providers can work with you to manage any symptoms that may arise. This may involve referring you to; Endocrinology Physical therapy Occupational therapy Speech therapy Psychology A fertility specialist for counseling, and later for family planning Genetic counseling if you want to become pregnant I knew you BEFORE I FORMED YOU IN YOUR MOTHER’S WOMB