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Turner syndrome is a genetic condition that affects girls and women. It can cause underdeveloped female sex characteristics, short stature, heart problems, osteoporosis, diabetes and more. Learn about the symptoms, causes and treatment of Turner syndrome.
Turner syndrome is a condition in which a girl or woman is partially or completely missing an X chromosome. Learn about the symptoms, diagnosis, and treatment of this disorder from the National Institute of Child Health and Human Development.
Klinefelter syndrome (KS) is a condition where males have an extra X chromosome (47,XXY). It can cause physical, language, learning, social and behavioral problems. Learn more about the symptoms, diagnosis and treatment of KS.
Learn about the common treatments for Turner syndrome, such as growth hormone and estrogen replacement therapy, that can help minimize its effects. Find out how to access regular health checks and specialists for various health problems related to Turner syndrome.
Turner syndrome is a genetic condition that affects girls when they are missing part or all of an X chromosome. Learn how this error happens during egg or sperm ...
A main focus is the cardiovascular effects of Turner syndrome in women. Section research has shown that malformations of cardiac veins are more common than originally thought, occurring in more than 20% of women with Turner syndrome. Research also discovered a new abnormality of the aorta, common in up to half of women with Turner syndrome.
Learn about the common signs and symptoms of Fragile X syndrome, a genetic disorder that affects intelligence, learning, behavior, and physical appearance. Find out how the syndrome can vary in severity and affect males and females differently.
Learn about the symptoms of Prader-Willi syndrome (PWS), a genetic disorder that affects feeding, metabolism, growth, and behavior. Find out how PWS symptoms develop in two stages and what complications they can cause.
The earlier in life that KS symptoms are recognized and treated, the more likely it is that the symptoms can be reduced or eliminated. 2 It is especially helpful to begin treatment by early puberty. Puberty is a time of rapid physical and psychological change, and treatment then can successfully limit symptoms.
Down syndrome is caused by an extra copy of chromosome 21, which occurs by chance during egg or sperm formation. There are three types of chromosomal changes that can cause Down syndrome: complete trisomy 21, mosaic trisomy 21, and translocation trisomy 21.