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Learn or gain valuable insights from a peer. Contact us, connect with someone by phone or email, or join the TSSUS private FB group. The Turner Syndrome Society advances knowledge, facilitates research, and provides support for all those touched by Turner syndrome.
The Turner Syndrome Society of the United States: Advancing knowledge, facilitating research, and supporting all those touched by Turner syndrome.
Turner syndrome is a common disorder that indiscriminately takes the lives of nearly every fetus it touches. There is hope for Turner syndrome. 1 in every 2,000 women and girls will be affected by TS. They are the survivors of Turner syndrome, and they require a lifetime of specialized care.
Simplify your Turner syndrome healthcare with easy-to-understand guidelines and checklists. Find out what specialists you should see, how often, and what tests they should recommend.
Turner syndrome (TS) is a chromosomal disorder caused by a partially or completely missing X chromosome. This condition affects only females. Most people have 46 chromosomes in each cell—23 from their mother and 23 from their father.
Established in 1987, the Turner Syndrome Society of the United States is a national non-profit self-help organization dedicated to advancing knowledge, facilitating research, and providing support for all people touched by Turner syndrome (TS).
Turner Syndrome (TS) is a randomly acquired chromosomal disorder affecting only women and girls, over two million of them. TS should be detected during a girl’s first few years of life, if not before or at birth, for the best possible outcomes.
Turner Syndrome is a random chromosomal disorder affecting only women and over two million of them. It should be detected during a girl’s first few years of life, if not at birth, for the best possible outcomes.
The Turner Syndrome Support Society (UK) is a national charity caring for the needs of girls and women with Turner Syndrome throughout the United Kingdom.
The Turner Syndrome Global Alliance (TSGA) aims to have a direct impact on the lives of girls, women, and families living with Turner syndrome (TS) by working to include TS in the national conversation on genetic research.