Turner syndrome

Turner syndrome
Definition:
Turner syndrome is a genetic condition that occurs only in females. Female cells normally have two X chromosomes. In Turner syndrome, the girl's cells are missing an X chromosome, or part of an X chromosome.
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Turner syndrome - Turner syndrome is a genetic disorder seen in girls that causes them to be shorter than others and to not mature sexually as they grow into adulthood. The severity of these problems varies among affected individuals.
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Turner syndrome. People with this syndrome have 45 chromosomes, including one missing or incomplete X chromosome, instead of 46. High blood pressure, heart problems and a number of other health conditions may result from this disorder.
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Turner Syndrome Support Society
British Medical Journal
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Monosomy X (Turner Syndrome)
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Turner Syndrome - Source:MedicineNet
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Nutropin (somatropin [rDNA] origin for injection) Indicated for the treatment of growth failure associated with Turner syndrome.
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In Turner syndrome, a defect that results in abnormal female sexual development, only one X chromosome is present. In Klinefelter's syndrome, a disorder that affects males, at least one extra X chromosome is present.
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A missing X chromosome causes Turner syndrome and an extra X in a male causes Klinefelter syndrome. Other abnormalities are caused by extra or missing pieces of chromosomes.
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