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  2. Primary aldosteronism - Wikipedia

    en.wikipedia.org/wiki/Primary_aldosteronism

    About 35% of the cases are caused by a single aldosterone-secreting adenoma, a condition known as Conn's syndrome. [ 7 ] [ 8 ] Many patients experience fatigue, potassium deficiency and high blood pressure which may cause poor vision, confusion or headaches .

  3. Multiple endocrine neoplasia type 2 - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    Multiple endocrine neoplasia type 2 (also known as "Pheochromocytoma (codons 630 and 634) and amyloid producing medullary thyroid carcinoma", [1] "PTC syndrome," [1] and "Sipple syndrome" [1]) is a group of medical disorders associated with tumors of the endocrine system. The tumors may be benign or malignant .

  4. Adrenal tumor - Wikipedia

    en.wikipedia.org/wiki/Adrenal_tumor

    Pheochromocytoma is a neoplasm composed of cells similar to the chromaffin cells of the mature adrenal medulla. Pheochromocytomas occur in patients of all ages, and may be sporadic, or associated with a hereditary cancer syndrome, such as multiple endocrine neoplasia (MEN) types IIA and IIB, neurofibromatosis type I, or von Hippel–Lindau ...

  5. Adrenocortical adenoma - Wikipedia

    en.wikipedia.org/wiki/Adrenocortical_adenoma

    Functional adrenocortical adenomas demonstrate symptoms consistent with mixed endocrine syndromes. In most reported cases of adrenocortical adenoma, patients have presented with one or multiple endocrine syndromes such as hyperaldosteronism / Conn's Syndrome , [ 3 ] hypercortisolism / Cushing's syndrome , [ 4 ] hyperandrogenism / feminization ...

  6. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    If a patient has the characteristic signs and symptoms of a pheochromocytoma and the decision is made to pursue additional biochemical (blood work) evaluation, the differential diagnosis is important as it is more likely to be something other than a pheochromocytoma given the relative frequency of 0.8 per 100,000 person-years. [3]

  7. Multiple endocrine neoplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine_neoplasia

    In 1954 Wermer noted that this syndrome was transmitted as a dominant trait. [citation needed] In 1959 Hazard et al. described medullary (solid) thyroid carcinoma. [citation needed] In 1961 Sipple described a combination of a pheochromocytoma, medullary thyroid carcinoma and parathyroid adenoma. [citation needed]

  8. Jerome W. Conn - Wikipedia

    en.wikipedia.org/wiki/Jerome_W._Conn

    After extensive research he had found a condition he called primary hyperaldosteronism, later called Conn syndrome. There were elevated levels of aldosterone in her circulation, coming from a hormone producing adrenal adenoma. Conn wrote a total of 284 articles and book chapters and was recognized as a tutor stimulating others in research.

  9. Batten disease - Wikipedia

    en.wikipedia.org/wiki/Batten_disease

    Over time, affected children experience mental impairment, worsening seizures and progressive loss of sight, speech and motor skills. Batten disease is a terminal disease; life expectancy varies depending on the type or variation. [7] [8] Females with juvenile Batten disease show first symptoms a year later than males, but on average die a year ...