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926 Possible Causes for Renal or Metabolic Acidosis

  • Acidosis

    The complications of chronic renal failure include fluid overload, electrolyte imbalance, metabolic acidosis , anaemia, and renal osteodystrophy.[] , e.g., ammonium chloride, acetazolamide, bile acid sequestrants Renal failure Metabolic Acidosis with an Elevated Anion Gap: lactic acidosis ketoacidosis chronic renal failure[] Threshold of metabolic acidosis associated with newborn complications.[]

  • Metabolic Acidosis

    We herein report the case of a patient with acute renal failure and metabolic acidosis caused directly by consumption of oxalic acid.[] They are associated with metabolic disorders related to renal insufficiency, among which metabolic acidosis is a major contributor.[] Here we report the first case of metabolic acidosis and renal injury caused by isoniazid at normal prescribed dose.[]

  • Renal Tubular Acidosis

    We diagnosed him with relapse of metabolic acidosis caused by renal tubular acidosis.[] […] syndrome characterized by hyperchloremic metabolic acidosis secondary to an abnormality in renal acidification.[] Indeed, in classical (type I) renal tubular acidosis the urine is often alkaline. Thus renal tubular acidosis is a metabolic acidosis of renal tubular origin.[]

  • Distal Renal Tubular Acidosis

    A Japanese infant presenting with vomiting, failure to thrive, metabolic acidosis, and hyperammonemia was finally diagnosed with autosomal recessive distal renal tubular acidosis[] OBJECTIVE: Distal renal tubular acidosis (dRTA) is characterized by metabolic acidosis due to impaired renal acid excretion.[] Renal tubular acidosis is a common cause of normal anion gap metabolic acidosis but these disorders can be easily missed or misdiagnosed.[]

  • Acute Alcohol Intoxication

    In addition to metabolic acidosis, acute renal failure and neurologic disease can occur in some of the intoxications.[] Metabolic acidosis is compounded by respiratory failure. Patients may also present with hypothermia.[] Administration of base is recommended to treat the metabolic acidosis and promote the renal removal of formate ( 15, 61 ).[]

  • Vitamin D Deficiency

    , familial hypophosphatemic (vitamin D–resistant) rickets, chronic metabolic acidosis, hyperparathyroidism, hypoparathyroidism, inadequate dietary calcium, and disorders or[] It is a common cause of rickets and osteomalacia, but these disorders may also result from other conditions, such as chronic kidney disease, various renal tubular disorders[]

  • Proximal Renal Tubular Acidosis

    […] failure and in experimental metabolic acidosis in animals.[] This case demonstrates that early administration of alkali therapy and sustained correction of acidosis, even if inadequate to correct the metabolic acidosis, can markedly[] […] by metabolic acidosis, a severe disturbance of extracellular pH homeostasis, due to renal impaired acid excretion.[]

  • Autosomal Dominant Distal Renal Tubular Acidosis

    Often, people who initially have incomplete distal renal tubular acidosis develop metabolic acidosis later in life.[] […] tubular acidosis (AD dRTA) is an inherited form of distal renal tubular acidosis (dRTA; see this term) characterized by hyperchloremic metabolic acidosis often but not always[] The characteristic symptom is a mild metabolic acidosis caused by tubular dysfunction.[]

  • Hyperuricemia

    HTN, polycystic kidney disease, chronic renal failure Metabolic/endocrine Dehydration, lactic acidosis, ketosis, hypothyroidism Miscellaneous Obesity, toxemia of pregnancy[] Additional renal effects of hyperuricemia include metabolic acidosis caused by defective lactic acid excretion which in turn exacerbates the hyperuricemia due to reduced urate[] […] purines Hematologic Myelo- and lymphoproliferative disorders Miscellaneous Obesity, hypertriglyceridemia, enzyme abnormalities Causes for decreased urate excretion Drugs Renal[]

  • Hypoglycemia

    acidosis, cardiomyopathy and muscle weakness (van den Berghe, 1996).[] DEFECTS IN FATTY ACID METABOLISM (NON-KETOTIC) Abnormalities in fatty acid oxidation and ketone body formation result in nonketotic hypoglycemia triggered by periods of fasting[] Other disorders : PEP carboxykinase deficiency is very rare; begins in neonatal period and involves FTT, microcephaly, developmental delay, seizures, hepatomegaly, renal tubular[]

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