Turner Syndrome What Is Turner Syndrome?


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Turner Syndrome Causes and Symptoms

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Turner Syndrome What Is Turner Syndrome?

Turner syndrome happens when a baby assigned female at birth is born with one missing or partial X chromosome. It causes a variety of symptoms and features, like short stature and issues with ovary function. There's no cure, but treatment involves managing hormone levels and other health conditions.


A 7yearold girl with pterygium colli associated with Turner syndrome. Download Scientific

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Symptoms & Characteristics Turner Syndrome

Turner syndrome, a condition that affects only females, results when one of the X chromosomes (sex chromosomes) is missing or partially missing. Turner syndrome can cause a variety of medical and developmental problems, including short height, failure of the ovaries to develop and heart defects.


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Turner Syndrome Symptoms, Causes, Diagnosis and Treatment Natural Health News

Turner syndrome has characteristic clinical features which include short stature and premature ovarian failure in a phenotypic female. Variable phenotype; obvious stigmata such as neck webbing affect only 20% to 30% of patients. Recent studies show that complex epigenetic factors and gene-gene interactions contribute to this specific phenotype.


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Turner Syndrome What Is Turner Syndrome?

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Turner syndrome affects approximately 1 in 2500 live female births and is a common cause of miscarriage (up to 10%). It affects 3% of females conceived but only 1% survive to birth. Turner syndrome develops when there is only one entire functional X chromosome. In approximately 50% of patients there is a single X chromosome ie 45,X.


WHAT DO YOU KNOW ABOUT TURNER SYNDROME?

Presentation Turner syndrome has a number of physical and psychological impacts, including short stature, heart defects, neck webbing, delayed or absent puberty, and infertility. The phenotype of Turner syndrome is affected by mosaicism, where cell lines with a single sex chromosome are combined with those with multiple.