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401 Essential hypertension. 401.0 Hypertension, malignant; 401.1 Hypertension, benign; 401.9 Hypertension, unspecified; 402 Hypertensive heart disease; 403 Hypertensive renal disease. 403.0 Malignant hypertensive renal disease; 403.1 Benign hypertensive renal disease; 404 Hypertensive heart and renal disease; 405 Secondary hypertension. 405.0 ...
Diminished or absent pulses, vascular bruits, hypertension, Takayasu retinopathy, and aortic regurgitation. [9] Giant cell arteritis: Headache, scalp tenderness, jaw claudication, and blindness. [10] Primary medium vessel vasculitis [8] Polyarteritis nodosa: Mononeuritis multiplex, nodules, purpura, livedo, and hypertension. [11] Kawasaki disease
Secondary hypertension (or, less commonly, inessential hypertension) is a type of hypertension which has a specific and identifiable underlying primary cause. It is much less common than essential hypertension , affecting only 5-10% of hypertensive patients.
Inactivation of the hepatic fructokinase results in asymptomatic fructosuria. [citation needed] Hereditary fructose intolerance (HFI) results in poor feeding, failure to thrive, chronic liver disease and chronic kidney disease, and death. HFI is caused by a deficiency of fructose 1,6-biphosphate aldolase in the liver, kidney cortex and small ...
A 2014 meta analysis found no increased risk of persistent pulmonary hypertension associated with exposure to SSRI's in early pregnancy and a slight increase in risk associates with exposure late in pregnancy; "an estimated 286 to 351 women would need to be treated with an SSRI in late pregnancy to result in an average of one additional case of ...
Acute liver failure is the appearance of severe complications rapidly after the first signs (such as jaundice) of liver disease, and indicates that the liver has sustained severe damage (loss of function of 80–90% of liver cells).
Café au lait spot characteristic of NF1 Diagnostic criteria of neurofibromatosis type I, requiring at least 2 of the mentioned items. [6]The following is a list of conditions and complications associated with NF-1, and, where available, age range of onset and progressive development, occurrence percentage of NF-1 population, method of earliest diagnosis, and treatments and related medical ...
Other severe side effects include high white blood cell counts and blood clots. [8] Use during pregnancy is contraindicated due to the risk of birth defects. [8] [1] It is in the retinoid family of medications. [9] Tretinoin was patented in 1957 and approved for medical use in 1962. [13] It is on the World Health Organization's List of ...