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Differential Diagnosis For PVT/Anemia in an Infant

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List of current finding(s):

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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