Gonadal dysgenesis: The abnormal development of gonads which means that the sex hormones are not being produced. The gonads are the primary reproductive organs - testes in males and ovaries in females. These organs produced sperm and eggs as well as sex hormones - testes produce the male hormone called testosterone and ovaries produce the female hormone called estrogen. Abnormal gonad development and hence lack of sex hormones can affect sexual differentiation between males and females and puberty may be delayed or fail to occur altogether. More detailed information about the symptoms, causes, and treatments of Gonadal dysgenesis is available below.
See full list of 8 symptoms of Gonadal dysgenesis
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The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Gonadal dysgenesis include:
See full list of 17 Clinical Trials for Gonadal dysgenesis
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Gonadal dysgenesis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Gonadal dysgenesis, or a subtype of Gonadal dysgenesis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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