Androgen insensitivity syndrome ultrasound: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Androgen insensitivity syndrome}} | {{Androgen insensitivity syndrome}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{ARK}} | ||
==Ultrasound== | ==Ultrasound== | ||
Evaluation of neonatal ambiguity is described in more detail in the [[intersex]] article. It typically consists of pelvic ultrasound to determine presence or absence of uterus and gonads. | *Radiology findings in the “predominantly male” phenotype including impaired development of the prostate and of the wolffian duct derivatives demonstrated by ultrasonography or genitourography. | ||
*Evaluation of neonatal ambiguity is described in more detail in the [[intersex]] article. It typically consists of pelvic ultrasound to determine presence or absence of uterus and gonads. | |||
==References== | ==References== | ||
Revision as of 13:12, 6 July 2017
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Androgen insensitivity syndrome Microchapters |
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Differentiating Androgen insensitivity syndrome from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Androgen insensitivity syndrome ultrasound On the Web |
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American Roentgen Ray Society Images of Androgen insensitivity syndrome ultrasound |
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Directions to Hospitals Treating Androgen insensitivity syndrome |
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Risk calculators and risk factors for Androgen insensitivity syndrome ultrasound |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aravind Reddy Kothagadi M.B.B.S[2]
Ultrasound
- Radiology findings in the “predominantly male” phenotype including impaired development of the prostate and of the wolffian duct derivatives demonstrated by ultrasonography or genitourography.
- Evaluation of neonatal ambiguity is described in more detail in the intersex article. It typically consists of pelvic ultrasound to determine presence or absence of uterus and gonads.