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22 Possible Causes for Congenital Nonspherocytic Hemolytic Anemia, Uric Acid Increased

  • Hereditary Spherocytosis

    From Wikidata Jump to navigation Jump to search congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia edit English hereditary[…][wikidata.org]

  • Autoimmune Hemolytic Anemia

    Red blood cell (RBC) autoantibodies are a relatively uncommon cause of anemia. However, autoimmune hemolytic anemia (AIHA) must be considered in the differential diagnosis of hemolytic anemias, especially if the patient has a concomitant lymphoproliferative disorder, autoimmune disease, or viral or mycoplasmal infection.[…][ncbi.nlm.nih.gov]

  • Glycogen Storage Disease Type 1

    Add Allopurinol to reduce uric acid levels which occurs because of the decrease in renal clearance and the increased production of uric acid as glycogen is not broken down[en.wikibooks.org] […] nucleic acid degradation pathway and resulting in increased uric acid, the end product.[emedicine.medscape.com] Uric acid, ketoacids, and free fatty acids further increase the anion gap.[en.wikipedia.org]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    Summary Epidemiology PK deficiency is the most frequent cause of congenital nonspherocytic hemolytic anemia with a prevalence estimated at 1/20,000 in the general white population[orpha.net] However, inosine, which is a naturally occurring substance, increases plasma uric acid levels ( 38 ).[nature.com] anemia and congenital hemolytic anemia.[malacards.org]

  • Hexokinase Deficiency

    The findings were entirely different from those of subsequently reported cases with congenital, nonspherocytic hemolytic anemia associated only with a specific deficiency[jamanetwork.com] Uric Acid), and the patient presents Hyperuricemia.[biochemistryquestions.wordpress.com] […] recessive inheritance ; Cholecystitis ; Cholelithiasis ; Congenital onset ; Hyperbilirubinemia ; Jaundice ; Nonspherocytic hemolytic anemia ; Normochromic anemia ; Normocytic[mousephenotype.org]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    .: Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (type Nordhorn). II.[link.springer.com] 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] World Health Organization classification of G6PD: Class 1: congenital nonspherocytic hemolytic anemia: rare.[unboundmedicine.com]

  • Refractory Megaloblastic Anemia

    nonspherocytic hemolytic anemia * (n) 先天性貧血 P614 ** せんてんせいひんけつ PubMed , Scholar , Google , WikiPedia congenital anemia * (n*) 先天性溶血性貧血 *** せんてんせいようけつせいひんけつ シソーラス PubMed ,[lsd-project.jp] […] degree of in effective erythropoiesis · Haptoglobins, Uric acid and alkaline phosphatase levels – Decreased. · Serum methylmalonate and homocystein levels - Vitamin B-12[sites.google.com] , WikiPedia 【類義語】 先天性赤芽球癆 , 先天性形成不良性貧血 congenital hypoplastic anemia * (n) 先天性非球状赤血球性溶血性貧血 * せんてんせいひきゅうじょうせっけっきゅうせいようけつせいひんけつ シソーラス PubMed , Scholar , Google , WikiPedia congenital[lsd-project.jp]

  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    , Hemolytic, Congenital Nonspherocytic Genetic Diseases, X-Linked Kidney Diseases Glycogen Storage Disease Type VII Multiple Acyl Coenzyme A Dehydrogenase Deficiency Genetic[clinicaltrials.gov] acid Cori's disease lab data Cori's disease clinical sever hypoglycemia, ketosis, hepato(nephro)megaly increased # of short outer branches of glycogen Cori's disease Amylo[quia.com] Storage Disease Type IV Glycogen Storage Disease Type III Cardiomyopathies Hyperammonemia Rhabdomyolysis Mitochondrial Myopathies Carbohydrate Metabolism, Inborn Errors Anemia[clinicaltrials.gov]

  • Helsmoortel-van der Aa Syndrome

    Nonspherocytic Hemolytic Anemia with Genital and Other Abnormalities Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinemia Light Fixation Seizure Syndrome Linear[rgd.mcw.edu] […] in uric acid levels and in frequency of gout of 2.9% in tolvaptan-treated subjects vs 1.4% in placebo.[dovepress.com] Also, the increased incidence of uric acid nephrolithiasis as a factor in producing renal colic must be considered when evaluating acute pain in the population at risk.[wjgnet.com]

  • Retinitis

    […] amaurosis AD/AR 34 235 HGSNAT Mucopolysaccharidosis (Sanfilippo syndrome), Retinitis pigmentosa AR 43 72 HK1 Hemolytic anemia, nonspherocytic, due to hexokinase deficiency[blueprintgenetics.com] Factors predisposing to kidney stones include recent reduction in fluid intake, increased exercise with dehydration, medications that cause hyperuricemia (high uric acid)[medicinenet.com] Depending on the type of stone, urine and blood tests may be necessary to measure levels of calcium, uric acid, hormones, and other substances that may increase the risk of[msdmanuals.com]

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