Turners syndrome research paper

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Turner syndrome is a chromosomal condition that affects development in females. The most common feature of Turner syndrome is short stature, which becomes evident by about age 5. An early loss of ovarian function ovarian hypofunction or premature ovarian failure is also very common. The ovaries develop normally at first, but egg cells oocytes usually die prematurely and most ovarian tissue degenerates before birth. Many affected girls do not undergo puberty unless they receive hormone therapy, and most are unable to conceive infertile. A small percentage of females with Turner syndrome retain normal ovarian function through young adulthood.
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Turner Syndrome Example | Graduateway

Most important clinical features of TS are short stature and gonadal failure. Approximately one third of girls with TS may undergo spontaneous puberty. Case report: The patient was diagnosed with TS at the age of 4 years, upon a diagnostic work-up for dysmorphic features. She presented with normal height and normal growth velocity so that Growth Hormone GH therapy was not started. She was referred to our Department at the age of 7 years and 10 months, because of vaginal bleeding.
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Turner's Syndrome Research Paper

Your contributions will help us continue to deliver the stories that are important to you. But enough is enough. At 28, Turner Syndrome continues to dominate my life and now the time is right to step out from the invisible wall I seem to have built around myself and reveal my true identity.
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While we are building a new and improved webshop, please click below to purchase this content via our partner CCC and their Rightfind service. You will need to register with a RightFind account to finalise the purchase. Objective The aim of the Journal of Pediatric Endocrinology and Metabolism JPEM is to diffuse speedily new medical information by publishing clinical investigations in pediatric endocrinology and basic research from all over the world. JPEM is the only international journal dedicated exclusively to endocrinology in the neonatal, pediatric and adolescent age groups.
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