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12 Possible Causes for Aplastic Crisis, Intermittent Jaundice, Uric Acid Increased

  • Hereditary Spherocytosis

    In patients with a congenital hemolytic anemia, infection with this virus can cause an aplastic crisis.[] Abstract Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice[] Dubin-Johnson syndrome is a chronic, benign, intermittent jaundice, mostly of conjugated hyperbilirubinemia.[]

  • Sickle Cell Disease

    crisis).[] Each individual with SCD is unique, but the most common features are: Anemia (may cause fatigue and decreased endurance), reticulocytosis, and jaundice Intermittent acute[] Consequences of hemolysis may include chronic anemia, jaundice, predisposition to aplastic crisis, cholelithiasis, and delayed growth and sexual maturation.[]

  • Refractory Megaloblastic Anemia

    […] anemia Aplastic anemia crisis Bacteremia / Septicemia Chemotherapy , cancer (anti-neoplastic) Chronic alcoholism Chronic liver disease Chronic renal failure Combined system[] […] degree of in effective erythropoiesis · Haptoglobins, Uric acid and alkaline phosphatase levels – Decreased. · Serum methylmalonate and homocystein levels - Vitamin B-12[] 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.[]

  • Leukemoid Reaction

    […] anemia (AA)再生不良性貧血 apoptosis アポトーシス autoimmune hemolytic anemia溶血性貧血 autologous transplantation自家移植 b blastic crisis (BC)急性転化 bone marrow aspiration骨髄穿刺 bone marrow biopsy[] .  In CML there is increase in  uric acid level  lactate dehydrogenase.  Increase in the level of angiogenic factors 40.  Entire chromosomal complement is evaluated to[] […] for 4 days, progressive pallor and jaundice for 3 days, bone pains, facial puffiness and edema of lower limbs for 2 days.[]

  • Hexokinase Deficiency

    An aplastic crisis occurs secondary to bone marrow suppression, usually by parvovirus infection or folate deficiency.[] Uric Acid), and the patient presents Hyperuricemia.[] Intermittent jaundice and premature pigment gallstones are common. Splenomegaly is characteristic (palpable in 75% to 80% of cases).[]

  • Familial Pseudohyperkalemia

    crisis?[] Microalbuminuria Increased WBC count Increased C-reactive protein Increased fibrinogen Increased pro inflammatory cytokines Increased uric acid Type 2 DM Fatty Liver HTN and[] Patients with HC1 may present later in life with macrocytosis, anemia, reticulocytosis, intermittent jaundice, gallstones, a palpable spleen tip, stomatocytosis, or because[]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    The unusual initial aplastic feature of this anemia could be the result of a transient erythroblastopenia due to the viral agent, at the origin of the G6PD crisis on a background[] 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.[] 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[]

  • Pneumatosis Vaginalis

    The most likely diagnosis is a. acute splenic sequestration crisis b. aplastic crisis c. hemolytic crisis d. acute leukemia e. superimposed iron deficiency Definition Term[] LESCH-NYHAN SYNDROME: Deficiency of HGPRT (Hypoxanthine-Guanine Phospho-ribosyltransferase ------ Hyperuricemia, uric acid kidney stones Choreoathetosis Mental retardation[] He is receiving intermittent orogastric feeding of expressed human milk and supplemental parenteral nutrition.[]

  • Optic Nerve Edema-Splenomegaly Syndrome

    If the reticulocyte count is low consider aplastic crisis.[] , Blood Thyroid Stimulating Hormone Increased, Blood Uric Acid Increased, Blood Urine, Blood Urine Present, Body Height Below Normal, Body Height Increased, Body Temperature[] Presents in teens with intermittent jaundice and hepatomegaly.[]

  • Fanconi Renotubular Syndrome Type 3

    Aplastic crisis due to Infection by parvovirus2.Hemolytic crisis3.Gall stonesTreatmentSplenectomyHEREDITARY SPHEROCYTOSISGenetic defects affecting ankyrin, spectrin, usually[] Urolithiasis from the uricosuria has only rarely been reported, probably because the urine flow and pH are increased, inhibiting uric acid crystallization.[] The absence of jaundice, hypoglycaemia and a history of vomiting made hereditary fructose intolerance unlikely.[]

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