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  2. Hypopituitarism - Wikipedia

    en.wikipedia.org/wiki/Hypopituitarism

    Levels of LH/FSH may be suppressed by a raised prolactin level, and are therefore not interpretable unless prolactin is low or normal. In men, the combination of low LH and FSH in combination with a low testosterone confirms LH/FSH deficiency; a high testosterone would indicate a source elsewhere in the body (such as a testosterone-secreting ...

  3. What Is Low Testosterone & What Causes It? - AOL

    www.aol.com/low-testosterone-causes-125700734.html

    Poor pituitary production of LH is thought to be implicated in obesity-associated testosterone deficiency. One study revealed that altering a BMI from 30 to 25 kg/m2 could result in a 13 percent ...

  4. Hypogonadotropic hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadotropic_hypogonadism

    If the patient has hypothalamic GnRH deficiency, LH and FSH will gradually appear in response to the exogenous GnRH but in pituitary cases of HH, a minimal response will be generated. [16] Typically, CHH is diagnosed in adolescence due to a lack of pubertal development, but it can be possible to diagnose in male neonates.

  5. Sheehan's syndrome - Wikipedia

    en.wikipedia.org/wiki/Sheehan's_syndrome

    Sheehan's syndrome, also known as postpartum pituitary gland necrosis, occurs when the pituitary gland is damaged due to significant blood loss and hypovolemic shock (ischemic necrosis) or stroke, originally described during or after childbirth leading to decreased functioning of the pituitary gland (hypopituitarism). [1]

  6. Autoimmune hypophysitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_hypophysitis

    Autoimmune hypophysitis can lead to deficiencies in one or more pituitary hormones, causing central diabetes insipidus if the posterior pituitary gland is affected as well as central adrenal insufficiency and central hypothyroidism if the anterior pituitary gland is affected. [1]

  7. Kallmann syndrome - Wikipedia

    en.wikipedia.org/wiki/Kallmann_syndrome

    The underlying cause is due to the defective migration of GNRH neurons from olfactory placode to hypothalamus, leading to congenital GNRH deficiency. This leads to olfactory problems such as anosmia, optic defects like color blindness, and results in hypothalmic deficiencies associated with low levels of LH, affecting sex hormone testosterone ...

  8. Hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadism

    In any case, the LH and FSH levels will rise in cases of primary hypogonadism or menopause, while they will be low in women with secondary or tertiary hypogonadism. [ 7 ] Hypogonadism is often discovered during evaluation of delayed puberty , but ordinary delay, which eventually results in normal pubertal development, wherein reproductive ...

  9. Pituitary apoplexy - Wikipedia

    en.wikipedia.org/wiki/Pituitary_apoplexy

    Several other hormonal deficiencies may develop in the subacute phase. 50% have a deficiency in thyroid-stimulating hormone (TSH), leading to hyposecretion of thyroid hormone by the thyroid gland and characteristic symptoms such as fatigue, weight gain, and cold intolerance. 75% develop a deficiency to gonadotropins (LH and FSH), which control ...