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Differential Diagnosis For Anemia in Children

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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
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
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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