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  1. ... decision about whether to proceed with surgical intervention. 46,XY DSD Testosterone biosynthetic defects Neonates are usually (but ... of delivering multi-disciplinary care to people with 46 XY DSD. J Pediatr Urol. 2012 Feb;8(1): ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  2. ... defects. INVESTIGATIONS Karyotype is normal female 46,XX. 46,XY complete gonadal dysgenesis SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS ... stature or congenital heart defects. INVESTIGATIONS Karyotype is 46,XY. Complete androgen insensitivity SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  3. ... achieved and adrenal crises can usually be avoided. 46,XY DSD and sex chromosomal DSD The outcome depends ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  4. ... DSD can be classified as sex chromosome DSD, 46,XY DSD, or 46,XX DSD . Sex chromosome DSD ... chromosomal arrangement is present (e.g., 45,X/46, XY). 46,XX DSD are conditions characterised by excess ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  5. ... therapy. serum TSH: normal serum prolactin: normal karyotype: 46,XY More karyotype Any permutation with a Y chromosome ... is taking any form of hormonal therapy. karyotype: 46,XY serum LH: normal to slightly elevated More serum ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  6. ... DSD can be classified as sex chromosome DSD, 46,XY DSD, or 46,XX DSD . ◊ Sex chromosome DSD ... chromosomal arrangement is present (e.g., 45,X/46, XY). ◊ 46,XX DSD are conditions characterised by excess ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  7. ... due to chimerism (which is rare). 45,X/46,XY mixed gonadal dysgenesis is due to post-meiotic ... Y chromosome in one cell lineage. 46,XX/46,XY chimerism results from the fusion of two zygotes. ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  8. ... therapy. » serum TSH: normal » serum prolactin: normal » karyotype: 46,XY Any permutation with a Y chromosome requires removal ... is taking any form of hormonal therapy. » karyotype: 46,XY ◊ 17-alpha-hydrox ylase (CYP17) deficiency » serum LH: ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  9. ... therapy. » serum TSH: normal » serum prolactin: normal » karyotype: 46,XY Any permutation with a Y chromosome requires removal ... is taking any form of hormonal therapy. » karyotype: 46,XY ◊ 17-alpha-hydrox ylase (CYP17) deficiency Other tests ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  10. ... Monosomy for the Y-chromosome is nonviable. Those 46,XY fetuses that lose a Y chromosome relatively late ... Ltd 2018. All rights reserved. Turner syndrome Condition 46,XY complete gonadal dys ge nes is Complete androgen ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
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