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Feline hyperaldosteronism is a disease in cats. The symptoms are caused by abnormally high concentrations of the hormone aldosterone, [1] which is secreted by the adrenal gland. The high concentrations of aldosterone may be due directly to a disorder of the adrenal gland (primary hyperaldosteronism), or due to something outside of the adrenal ...
Cats can be affected by hyperaldosteronism. The most common signs in cats are muscle weakness and loss of eyesight, although only one of these signs may be present. [ 12 ] Muscle weakness is due to low potassium concentrations in the blood, and signs of muscle weakness, such as being unable to jump, may be intermittent. [ 12 ]
The size of the adrenal glands can be useful in diagnosis, studies have found that the size of the adrenal gland in diabetic cats without hypersomatotropism does not differ significantly from non-diabetic cats; [11] [12] [1] however adrenomegaly is not pathognomonic to hypersomatotropism and can occur with other conditions in cats such as ...
Two slices of an adrenal gland with a cortical adenoma, from a person with Conn's syndrome. The condition is due to: [14] Bilateral idiopathic (micronodular) adrenal hyperplasia: 66% of cases [1] Adrenal adenoma (Conn's disease): 33% of cases [1] Primary (unilateral) adrenal hyperplasia: 2% of cases
The symptoms of Cushing's in cats is similar to that of dogs. [8] For cats the most common reason for referral resulting in a diagnosis is diabetes mellitus. Abnormal dermatological findings were the most common reason for referral after physical examination in cats. [9] 80% of cats with Cushing's develop diabetes mellitus compared to 10% of ...
In individuals with GRA, there is unequal crossing over so that the 5' regulatory region of the 11-hydroxylase gene is fused to the coding region of the aldosterone synthase. [citation needed] The product of this hybrid gene is aldosterone synthase that is ACTH-sensitive [2] in the zona fasciculata of the adrenal gland. [3]
Approximately 50% of women over 40 years of age Moderate to severe myeloneuropathy Similar to male AMN phenotype, but later onset and milder presentation Adulthood Approximately 15% of women over 40 years of age Cerebral involvement Progressive dementia and decline Rare in childhood, more common in adults ~2% Adrenal involvement
Late onset congenital adrenal hyperplasia (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of congenital adrenal hyperplasia (CAH), [1] a group of autosomal recessive disorders characterized by impaired cortisol synthesis that leads to variable degrees of postnatal androgen excess.