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11 Possible Causes for Congenital Hemolytic Anemia, Intermittent Jaundice, Uric Acid Increased

  • Hereditary Spherocytosis

    Abstract Hereditary spherocytosis (HS) is a disease affecting the red blood cells membrane and belongs to the congenital hemolytic anemias.[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]

  • 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]

  • Refractory Megaloblastic Anemia

    Anemia; Congenital Hemolytic Anemia; Sickle Cell Disease; Thrombotic Microangiopathy; Unusual Anemias; and Transfusion Therapy.[books.google.de] […] 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]

  • Hypercholesterolemia

    Gout or increased uric acid.[circ.ahajournals.org] […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] 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]

  • Diabetic Enteropathy

    […] adrenal hyperplasia (E25.0) Ehlers-Danlos syndrome (Q79.6) hemolytic anemias attributable to enzyme disorders (D55.-) Marfan's syndrome (Q87.4) 5-alpha-reductase deficiency[aapc.com] […] 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] Typical symptoms of biliary colic include intermittent right upper abdominal pain, jaundice, or pancreatitis.[journal.diabetes.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] Intermittent jaundice and premature pigment gallstones are common. Splenomegaly is characteristic (palpable in 75% to 80% of cases).[web.archive.org]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    In this overview the connection between rigidity and accelerated destruction of the erythrocytes in congenital hemolytic anemias will be discussed.[content.iospress.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.[cjasn.asnjournals.org] 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]

  • Tyrosinemia

    […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] The tubular handling of phosphorus, uric acid, beta 2-microglobulin, and amino acids was disturbed. Low urinary osmolality was also seen.[ncbi.nlm.nih.gov] The acute onset may be dramatic, with hepatomegaly, jaundice, epistaxis, melaena, purpuric lesions, marked oedema, and the distinctive cabbage-like odour.[patient.info]

  • Beta-Ureidopropionase Deficiency

    […] adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase[icd10data.com] Plasmodium falciparum (malaria parasite) Along with many other disease causing parasites -Juvenile gout -No salvage of purines, therefore causing an increase in uric acid[quizlet.com] Intellectual disability, seizures, and periodic loss of balance and coordination (intermittent ataxia).[metascreen.vn]

  • Autosomal Dominant Mental Retardation 5

    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] Jaundice was intermittent but pruritus persisted during anicteric stages. The last observations were made at age 12.[findzebra.com]

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