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Hypothalamic disease is a disorder presenting primarily in the hypothalamus, which may be caused by damage resulting from malnutrition, including anorexia and bulimia eating disorders, [1] [2] genetic disorders, radiation, surgery, head trauma, [3] lesion, [1] tumour or other physical injury to the hypothalamus. The hypothalamus is the control ...
As not all ROHHAD patients develop the same symptoms, treatment plans vary between patients. Proper treatment of hypothalamic dysfunction and hypoventilation is the most critical aspect of ROHHAD management, as these symptoms have the greatest ability to cause death or behavioral problems if left uncontrolled. [5]
The symptoms depend on what part of the pituitary is affected. Lymphocytic adenohypophysitis (LAH) occurs when the anterior pituitary cells are affected by autoimmune inflammation resulting in either no symptoms, adrenal insufficiency (if the ACTH producing cells are affected), hypothyroidism (if the TSH producing cells are damaged), or ...
This treatment uses synthetic testosterone to increase circulating testosterone levels and reduce low T symptoms. TRT comes in several forms, including skin patches, topical gels, oral capsules ...
Plus, "other symptoms of low T—like fatigue, depression, mental fog, low libido, and loss of energy—can make you cranky," Staheli says. "It's the perfect storm." "It's the perfect storm."
The symptoms of chronic syndrome of inappropriate antidiuresis are more vague, and may include cognitive impairment, gait abnormalities, or osteoporosis. [2] The main treatment of inappropriate antidiuresis is to identify and treat the underlying cause, if possible.
The hypothalamus is located below the thalamus and is part of the limbic system. [1] It forms the basal part of the diencephalon. All vertebrate brains contain a hypothalamus. [2] In humans, it is about the size of an almond. [3] The hypothalamus has the function of regulating certain metabolic processes and other activities of the autonomic ...
Hypothalamic obesity (abbreviated HO or HyOb) is a rare condition that can be congenital or acquired. Congenital causes include Prader-Willi syndrome and mutations of LEP ( leptin gene), LEPR , POMC , MC4R , and CART .