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Differential Diagnosis For Anemia in Children
- 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
Babesiosis
Chronic malaria
Cytomegalic virus, congenital
Hookworm (Ancylostomiasis) disease
Parvovirus Infection/Parvovirus 19
Rubella, congenital
Syphilis, congenital
Malaria- Infected organ, Abscesses
Neonatal infections
Newborn Sepsis Syndrome
Pneumonia of newborn
Anemia of chronic infection- Neoplastic Disorders
Leukemia, acute
Leukemia, congenital- Allergic, Collagen, Auto-Immune Disorders
Hemolytic disease of newborn
Erythroblastosis fetalis
Hemolytic anemia, autoimmune
Juvenile rheumatoid arthritis/Stills d
Fetal/maternal RH incompatability
Anemia of rheumatoid arthritis
Celiac disease of childhood
Juvenile chronic arthritis (rheumatoid)
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
Vitamin E defic. in newborns
Vitamin E deficiency- Congenital, Developmental Disorders
Hemorrhagic disease of newborn
Anemia, congenital hemolytic
Cretinism, goitrous sporadic
Placenta insufficiency syndrome/infant
Meckel diverticulum/Peptic ulcer
Cretinism
Anemia, congenital aplastic
Anemia, hypoplastic, congenital
Congenital dyserythropoetic anemia
Folate malabsorption, congenital
Meckel diverticulum- Hereditary, Familial, Genetic Disorders
Erythrocyte membrane disorders
Hemoglobin E thalassemia
Sickle cell/thalassemia disease
Thalassemia major
Thalassemia minor
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
Stomatocytosis (RBC defect)
Fanconi's pancytopenia-dysmelia synd
Thalassemia-hemoglobin C disease
Rh-Null syndrome- Functional, Physiologic Variant Disorders
Premature baby/severe prematurity- Vegetative, Autonomic, Endocrine Disorders
Hypothyroidism, juvenile- Reference to Organ System
Anemia
Anemia, blood loss
Anemia, posthemorrhagic, newborn
Anemia of chronic disease
Malabsorption syndrome
Anemia, aplastic
Renal Failure Chronic
Hemolytic-uremic syndrome
Transient Erythroblastopenia Childhood (TEC)- Pathophysiologic
Fluid balance/pathophysiology- Drugs
Hypothyroidism, iodide
Drug induced anemia- 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, in children, Unspecified anaemia, Unspecified anemia
- External Links Related to Anemia in Children
- 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)