Turners syndrom - Lægehåndbogen på sundhed.dk
WEB12.04.2023. Indledning. Turners syndrom (TS) skyldes helt eller delvis mangel på det ene X-kromosom hos piger og kvinder. Næsten alle har lille højde og svigt af æggestokkene med risiko for manglende pubertetsudvikling; andre symptomer varierer.
Turner syndrom - Netdoktor
WEBOpdateret: 30. November 2018. Forfatter: Claus H. Gravholt, Speciallæge i intern medicin. Hvad er Turner syndrom? Turner syndrom er en genetisk tilstand, som man kun ser hos piger og kvinder, der er født med et manglende eller ændret X-kromosom. Syndromet er opkaldt efter den amerikanske læge Henry Turner.
Turner syndrome - Wikipedia
WEBTurner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which a female is partially or completely missing an X chromosome (sex chromosome monosomy). Most people have two sex chromosomes (XX or XY). It only affects females. Signs and symptoms vary among those affected.
Turner syndrome - Symptoms & causes - Mayo Clinic
WEBden 11. feb. 2022 · 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.
Syndrome de Turner — Wikipédia
WEBLe syndrome de Turner est une maladie génétique rare caractérisée par l'absence totale (monosomie) ou partielle (délétion) du second chromosome (le chromosome X chez les femmes), de la 23 e paire dite « des chromosomes sexuels », qui diffère chez les filles XX, et les garçons XY.
Turner Syndrom - Turnerforeningen
WEBTurner Syndrom (TS) er en kønskromosomfejl, som kun optræder hos piger/kvinder. De mangler det ene af de to kønskromosomer, som har indflydelse på højden og på udvikling af æggestokkene. Syndromet er opkaldt efter den amerikanske læge Henry G. Turner, som i 1938 beskrev 7 piger/kvinder med syndromet.
Syndrome de Turner - Pédiatrie - Édition professionnelle du …
WEBDans le syndrome de Turner, les filles naissent avec un de leurs deux chromosomes X partiellement ou complètement manquants. Le diagnostic repose sur les signes cliniques et est confirmé par l'analyse cytogénétique.
Turner syndrome: MedlinePlus Genetics
WEBTurner syndrome is a chromosomal condition that affects development in people who are assigned female at birth. Females typically have two X chromosomes, but in individuals with Turner syndrome, one copy of the X chromosome is missing or altered. The most common feature of Turner syndrome is short stature, which becomes evident by …
Turner Syndrome: What It Is, Causes, Symptoms & Treatment
WEBden 10. okt. 2023 · 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.
Turner syndrome - Diagnosis & treatment - Mayo Clinic
WEBden 11. feb. 2022 · Symptoms & causes. Diagnosis & treatment. Doctors & departments. On this page. Diagnosis. Treatment. Coping and support. Preparing for your appointment. Diagnosis. If, based on signs and symptoms, the doctor suspects that your child has Turner syndrome, a lab test will be done to analyze your child's chromosomes. The test …
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