File:Turner syndrome karyotype.jpg
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Turner syndrome (45,X)
Monosomy XO, 99% non-viable embryos, fail to sexually mature at puberty. Named after Henry Turner (1938), an American clinician who first described the condition.
|ICD-11 LD50.0 Turner syndrome - Karyotype missing one X chromosome (45, X0 or 45,XO/46,XX mosaicism) ; gonads: ovaries (streak); phenotype female with short stature, amenorrhea (hypergonadotrophic hypogonadism), absence of sexual development, webbed neck, low set ears, posterior hairline, widely-spaced nipples, short fourth metacarpals, and increased carrying angle at the elbow (cubitus valgus). Often associated with renal, cardiac and ocular abnormalities.|
Cite this page: Hill, M.A. (2021, May 6) Embryology Turner syndrome karyotype.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Turner_syndrome_karyotype.jpg
- © Dr Mark Hill 2021, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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|current||11:35, 13 May 2010||480 × 284 (12 KB)||S8600021||==Turner syndrome (45,X)== Monosomy XO, 99% non-viable embryos, fail to sexually mature at puberty. Named after Henry Turner (1938), an American clinician who first described the condition. Category:Chromosome Category:Genetics [[Category:Genita|