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Diagnosis and terminology in hypogonadism
Hypogonadism (testosterone deficiency) is a clinical and biochemical syndrome that stems from a
reduced production of testosterone and sperm cells by the testis. It can adversely affect multiple
bodily systems and is associated with a marked decrease in quality of life. Hypogonadism is primarily
classified according to it being a congenital or acquired disorder; the anatomical level of dysfunction:
at testicular (primary hypogonadism), hypothalamic- pituitary (secondary hypogonadism) or
combined levels and recognises affected men with idiopathic, metabolic or iatrogenic conditions
resulting in testosterone deficiency. Treatment decisions should include lifestyle measures and a holistic review of the patient.
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This chapter aims at:
1. Shedding some light on definitions and terminology in patients with
testosterone deficiency (hypogonadal patients).
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2. Outlining its epidemiology.
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3. Exploring the underlying pathophysiology.
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4. Discussing issues surrounding diagnosis.
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5. Drawing a conclusion