Hypogonadism differential diagnosis
Hypogonadism Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Hypogonadism differential diagnosis On the Web |
American Roentgen Ray Society Images of Hypogonadism differential diagnosis |
Risk calculators and risk factors for Hypogonadism differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Differentiating Hypogonadism from other Diseases
- Hypogonadism cardinal features are ambigous gonads in the newborn, delayed puberty in children and infertility in adults. These features are caused by many diseases that must be differentiated in order to provide appropriate treatment.
- These disease include:
- Congenital diseases: Klinefelter's syndrome, cryptorchidism and Kallmann syndrome.
- Acquired diseases causing primary hypogonadism: testicular torsion, orchitis and varicocele
- Acquired diseases causing secondary hypogonadism {| class="wikitable" ! rowspan="6" |Infertility ! ! ! |- ! rowspan="2" |Men !Hypogonadism ! |- !Primary ciliary dyskinesia ! |- | rowspan="3" |Women |Polycystic ovarian syndrome | |- |Pelvic inflammatory disease ! |- !Endometriosis ! |- | | | | |- | | | | |}