turner syndrome Turner syndrome or Ullrich-Turner syndrome (also known as gonadal dysgenesis[1]:550), 45 XO, encompasses several conditions in human females, of which monosomy X (absence of an total provoke chromosome, the Barr body) is most common. It is a chromosomal abnormality in which all or part of one of the sex chromosomes is fatalitying(p) (unaffected humans have 46 chromosomes, of which two are sex chromosomes). Normal females have two X chromosomes, and in Turner syndrome, one of those sex chromosomes is missing or has opposite abnormalities. In some cases, the chromosome is missing in some cells but not others, a condition referred to as mosaicism[2] or Turner mosaicism. Occurring in 1 in 2000[3] 1 in 5000 phenotypic females,[4] the syndrome manifests itself in a number of ways. There are trait physical abnormalities, such as short stature, swelling, broad chest, kickoff hairline, low-set ears, and webbed necks.[5] Girls with Turner syndrome typically experience gonadal dysfunction (non-working ovaries), which results in amenorrhea (absence of menstrual cycle) and sterility. Concurrent wellness concerns are also frequently present, including congenital heart disease, hypothyroidism (reduced hormone secretion by the thyroid), diabetes, vision problems, hearing concerns, and many autoimmune diseases.

[6] Finally, a specific pattern of cognitive deficits is often observed, with incident difficulties in visuospatial, mathematical, and memory areas.[7] Turners syndrome is named after Henry H. Turner. Signs and symptoms Lymphedema, orotund legs of a newborn with Turner syndrome Common symptoms of Turner syndrome accept: * Short stature * Lymphedema (swelling) of the hands and feet * Broad chest (shield chest) and widely set-apart nipples * Low hairline * Low-set ears * Reproductive sterility * Rudimentary ovaries gonadal mottle (underdeveloped gonadal structures that later become fibrosed) * Amenorrhoea, or the absence of a... If you want to get a full essay, order it on our website:
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