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  2. Hypopituitarism - Wikipedia

    en.wikipedia.org/wiki/Hypopituitarism

    Hypopituitarism is the decreased (hypo) secretion of one or more of the eight hormones normally produced by the pituitary gland at the base of the brain. [1] [2] If there is decreased secretion of one specific pituitary hormone, the condition is known as selective hypopituitarism. [3]

  3. Autoimmune hypophysitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_hypophysitis

    80% of patients with pituitary antibodies also have antibodies to thyroid gland or its hormones. [2] Likewise, 20% of autoimmune thyroid patients also have pituitary antibodies. [ 7 ] It follows that a subset of thyroid patients may have a disease related to autoimmune hypophysitis.

  4. Hypophysitis - Wikipedia

    en.wikipedia.org/wiki/Hypophysitis

    Her symptoms began 3 months postpartum, with lassitude (weakness/lack of energy), goitre (iodine deficiency) and amenorrhea (absence of a menstrual period). This was originally reported by Goudie and Pinkerton in Glasgow, UK. There have only been approximately just over 100 cases reported.

  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. Hypoprolactinemia - Wikipedia

    en.wikipedia.org/wiki/Hypoprolactinemia

    Hypoprolactinemia can result from autoimmune disease, [2] hypopituitarism, [1] growth hormone deficiency, [2] hypothyroidism, [2] excessive dopamine action in the tuberoinfundibular pathway and/or the anterior pituitary, and ingestion of drugs that activate the D 2 receptor, such as direct D 2 receptor agonists like bromocriptine and pergolide, and indirect D 2 receptor activators like ...

  7. Hypogonadotropic hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadotropic_hypogonadism

    CHH can be diagnosed in the male neonate with cryptorchidism (maldescended testes) and a micropenis as signs of GnRH deficiency. [4] There are no clear signs of CHH in female neonates. [ 4 ] Another clinical sign of CHH, more specifically Kallmann syndrome, is a lack of a sense of smell due to the altered migration of GnRH neurons on the ...

  8. Experts Reveal the 6 Surprising Indicators of Longevity You ...

    www.aol.com/experts-reveal-6-surprising...

    At times, he’ll post nudes, his bulging musculature courtesy of 800-pound leg presses, a strict diet (mostly vegan, no wine—too many calories), and some 100 supplements a day.

  9. Pituitary apoplexy - Wikipedia

    en.wikipedia.org/wiki/Pituitary_apoplexy

    [12] 60–80% require hydrocortisone replacement (either permanently or when unwell), 50–60% need thyroid hormone replacement, and 60–80% of men require testosterone supplements. Finally, 10–25% develop diabetes insipidus , the inability to retain fluid in the kidneys due to a lack of the pituitary antidiuretic hormone .

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