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27 Possible Causes for Anemia, Intermittent Jaundice, Uric Acid Increased

  • Hereditary Spherocytosis

    To date only three siblings with coinheritance of sickle cell anemia (SCA) and hereditary spherocytosis (HS) have been reported.[ncbi.nlm.nih.gov] Abstract Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice[ncbi.nlm.nih.gov] Dubin-Johnson syndrome is a chronic, benign, intermittent jaundice, mostly of conjugated hyperbilirubinemia.[ncbi.nlm.nih.gov]

  • Hepatorenal Syndrome

    Wui-Chiang Lee, Han-Chieh Lin, Ming-Chih Hou, Hsiao-Yi Lin, Fa-Yauh Lee, Sun-Sang Wang, Full-Young Chang and Shou-Dong Lee , Serum Uric Acid Levels in Patients With Cirrhosis[dx.doi.org] Although anemia is a non-rare condition in advanced liver cirrhosis, there is no publication regarding the potential or additive effects of anemia on HRS and renal dysfunction[ncbi.nlm.nih.gov] Severe circulatory dysfunction (mean arterial pressure usually is 70 mm Hg) and very low systemic vascular resistance. • Severe liver disease, with jaundice, coagulopathy,[scielo.mec.pt]

  • Primary Biliary Cirrhosis

    Autoimmune hepatitis (AIH) and primary biliary cirrhosis (PBC) associated with Evans syndrome; combination of autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic[ncbi.nlm.nih.gov] Twenty four hour urine demonstrated a low renal fractional tubular reabsorption of phosphate, increased fractional excretion of uric acid and generalized aminoaciduria.[ncbi.nlm.nih.gov] Reddy AN, Grosberg SJ, Wapnick S: Intermittent cholestatic jaundice and nonmetastatic prostatic carcinoma. Arch Intern Med 1977;137:1616–1618.[clevelandclinicmeded.com]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    An acid urine pH favors production of poorly soluble uric acid over the more soluble urate, increasing the risk for precipitation of intratubular uric acid crystals.[doi.org] In addition, he was found to have acute hemolytic anemia due to previously undiagnosed G6PD deficiency.[ncbi.nlm.nih.gov] To determine whether you have an inherited G6PD deficiency When a child experienced persistent jaundice as a newborn for unknown reasons; when you have had one or more intermittent[labtestsonline.org]

  • Refractory Megaloblastic Anemia

    No explanation of the cause of the megaloblastic anemia was discovered in the remaining 25 cases. 2.[bloodjournal.org] […] degree of in effective erythropoiesis · Haptoglobins, Uric acid and alkaline phosphatase levels – Decreased. · Serum methylmalonate and homocystein levels - Vitamin B-12[sites.google.com] He has a fever and you note jaundice. You order an ultrasound of his abdomen and find multiple gallstones. Lab results: Hct .36 L/L; Hgb 120 g/L. PBS at right.[med-ed.virginia.edu]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    anemia and congenital hemolytic anemia.[malacards.org] However, inosine, which is a naturally occurring substance, increases plasma uric acid levels ( 38 ).[nature.com] jaundice and episodes of red/ dark urine Venous thrombosis in unusual locations (e.g., hepatic, cerebral, abdominal veins) Vasoconstriction : headache, pulmonary hypertension[amboss.com]

  • Hexokinase Deficiency

    Uric Acid), and the patient presents Hyperuricemia.[biochemistryquestions.wordpress.com] It is likely, although not certain, that in this patient nonspherocytic hemolytic anemia resulted from hexokinase deficiency.[ncbi.nlm.nih.gov] Intermittent jaundice and premature pigment gallstones are common. Splenomegaly is characteristic (palpable in 75% to 80% of cases).[web.archive.org]

  • Renal Impairment

    […] in uric acid excretion, serum creatinine, or BUN.[hyper.ahajournals.org] A blood test showed thrombocytopenia, anemia, and elevated C-reactive protein, alkaline phosphatase, and creatinine levels.[ncbi.nlm.nih.gov] Abstract Benign recurrent intrahepatic cholestasis (BRIC) is a rare autosomal recessive condition characterized by intermittent episodes of pruritus and jaundice that may[ncbi.nlm.nih.gov]

  • Diabetic Enteropathy

    […] risk of acute coronary ischaemia Autonomic dysfunction: Increased sympathetic nervous system activity Type 2 diabetes Uric acid levels 50% higher with neuropathy than without[neuromuscular.wustl.edu] Anemia and hypoalbuminemia were not detected in any of the patients with coexistent disease. Only 1 of the 3 patients had symptoms of diarrhea.[annals.org] Typical symptoms of biliary colic include intermittent right upper abdominal pain, jaundice, or pancreatitis.[journal.diabetes.org]

  • Hypercholesterolemia

    E70-E88 Metabolic disorders Type 1 Excludes androgen insensitivity syndrome ( E34.5- ) congenital adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias[icd10data.com] Gout or increased uric acid.[circ.ahajournals.org] We report the case of a male infant who had developed failure to thrive, jaundice, intermittent pruritus, and multiple diffuse symmetrical skin xanthomas at 1 year of age.[ncbi.nlm.nih.gov]

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