hypogonadism.docx - Running head HYPOGONADISM 1 Male Hypogonadism Students Name Professors Name Course Date HYPOGONADISM 2 Male Hypogonadism

hypogonadism.docx - Running head HYPOGONADISM 1 Male...

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Running head: HYPOGONADISM 1 Male Hypogonadism Student’s Name Professor’s Name Course Date
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HYPOGONADISM 2 Male Hypogonadism Hypogonadism refers to the state in which the gonads produce little or no testosterone hormone which plays a significant role in masculine growth. It can be inborn or may develop at a later stage from injury or infection. Pathophysiology at any level of the hypothalamic-pituitary- gonadal axis may result in hypogonadism. The causes include genetic diseases, head or testicular trauma, radiation injury among others. Determining the etiology of damage to the hypothalamic- pituitary-gonadal axis is essential because the prognosis and treatment options vary with these factors (Hackney, Anderson, & Dobridge 2017). Primary hypogonadism occurs due to pathophysiology of either Leydig cells or seminiferous tubules or both. Injury to Leydig cells results in decreased testosterone production, while seminiferous tubule involvement results in reduced or no spermatogenesis. Secondary
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