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Differential Diagnosis For PVT/Anemia in an Infant

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PVT/Anemia in an Infant
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Infectious Disorders (Specific Agent): Viral acute illness/Viremia; Newborn TORCH syndrome; Neonatal chlamydial pneumonia; Neonatal pneumonia, bacterial; Herpes simplex infection, newborn, gen; Immune deficiency , acquired (AIDS/HIV); Listeria hepatitis, newborn; Hemolysis with viral infection; Rubella hepatitis, newborn; Chronic malaria; Cytomegalic virus, congenital; Parvovirus Infection/Parvovirus 19; Rubella, congenital; Syphilis, congenital
Infected organ, Abscesses: Neonatal infections; Newborn Sepsis Syndrome; Pneumonia of newborn
Neoplastic Disorders: Leukemia, acute; Leukemia, congenital
Allergic, Collagen, Auto-Immune Disorders: Hemolytic disease of newborn; Erythroblastosis fetalis; Fetal/maternal RH incompatability; Anemia of rheumatoid arthritis; Celiac disease of childhood; Neonatal Lupus syndrome
Metabolic, Storage Disorders: Neonatal hyperbilirubinemia; Erythrocyte glycolytic enzyme defect; Glucose 6 PD deficiency; Anemia due to glutathione metab def; Erythrocyte nucleotide metabolism def't
Deficiency Disorders: Anemia of malnutrition; Deficiency disorders; Malnutrition, fetal; Failure to thrive/infancy; Folic acid deficiency anemia; Iron deficiency anemia; Iron deficient diet; Malnutrition/Starvation; Marasmus/inanition/cachexia infant; Pyridoxine deficiency anemia; Copper deficiency; Kwashiorkor (protein deficiency,severe); Scurvy, infantile
Congenital, Developmental Disorders: Hemorrhagic disease of newborn; Anemia, congenital hemolytic; Cretinism, goitrous sporadic; Placenta insufficiency syndrome/infant; Cretinism; Anemia, congenital aplastic; Anemia, hypoplastic, congenital; Congenital dyserythropoetic anemia; Folate malabsorption, congenital
Hereditary, Familial, Genetic Disorders: Erythrocyte membrane disorders; Sickle cell/thalassemia disease; Thalassemia major; Spherocytosis, crisis phase; Heinz body hereditary anemia; Hereditary hemolytic anemia syndromes; Hereditary sideroblastic anemia; Sickle cell anemia; Sickle cell-hemoglobin D disease; Spherocytosis, hereditary; Anemia, hereditary hemolytic,nonspher'c; Thalassemia-hemoglobin C disease
Vegetative, Autonomic, Endocrine Disorders: Hypothyroidism, juvenile
Reference to Organ System: Anemia, blood loss; Anemia, posthemorrhagic, newborn; Anemia of chronic disease; Malabsorption syndrome; Anemia, aplastic; Renal Failure Chronic
Pathophysiologic: Fluid balance/pathophysiology
Drugs: Hypothyroidism, iodide
Poisoning (Specific Agent): Fava-bean hemolysis (G6PD RBC defect); Lead poisoning in children; Lead poisoning; Mercury poisoning/infant/child
Synonyms: Anaemia, Anaemia (disorder), Anaemia unspecified, Anemia, Anemia (disorder), Anemia (dup) (disorder), anemia essential, Anemia unspecified, Anemia unspecified (disorder), Anemias, baby, Deep vein thrombos portal vein, Deep vein thrombosis of portal vein, infant, Infant (person), Infant child, Infant child (person), Infants, portal thrombosis, Portal vein thrombosis, Portal vein thrombosis (disorder), PVT Portal vein thrombosis, Pylethrombosis, thrombosis portal, Thrombosis portal vein, Unspecified anaemia, Unspecified anemia
External Links Related to PVT/Anemia in an Infant: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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