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Differential Diagnosis for Infant Seizures
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baby, Convulsion, Fit, infant, Infant (person), Infant child, Infant child (person), Infants, Seizure, Seizure (finding), Seizures, sz
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179 possible diagnoses found. Too many? Narrow results
Trauma Causes
Electromagnetic, Physics, trauma, Radiation Causes
Iatrogenic, Self Induced Disorders
Infectious Disorders (Specific Agent)
- Group B Streptococcus infection
- Cytomegalic virus
- Encephalitis, herpes simplex
- Encephalitis, viral
- Gram negative septicemia/endotoxemia
- Meningitis Bacterial
- Meningitis, Hemophilus
- Meningitis, pneumococcal
- Meningococcal meningitis
- Neonatal pneumonia, bacterial
- Herpes simplex infection, newborn, gen
- Encephalitis, Eastern equine
- Encephalitis, Murray valley
- Encephalitis, St Louis B
- Encephalitis, Western equine
- Gram negative (e coli) meningitis
- Leptospiral meningitis
- Listeria hepatitis, newborn
- Listeria meningitis
- Meningitis, staphylococcus aureus
- Plague meningitis
- Rubella panencephalitis
- Tetanus, neonatal
- West Nile fever/encephalitis
- Cytomegalic infection, disseminated
- Toxoplasma meningoencephalitis
- Cytomegalic virus, congenital
- Syphilis in pregnancy
- Syphilis, congenital
- Toxoplasmosis
- Toxoplasmosis, cerebral
- Toxoplasmosis, congental
- Encephalitis, California
- Encephalitis, equine, Venezuelan
- Encephalitis, Japanese B
- Encephalitis, powassan
- Tularemia meningitis
- Group B Strep Neonatal Sepsis
Infected organ, Abscesses
Neoplastic Disorders
Allergic, Collagen, Auto-Immune Disorders
Metabolic, Storage Disorders
- Enzyme defect/deficiency disorders
- Infant of diabetic mother
- Primary lactic acidemia/children
- Metabolic disorders
- Porphyria, acute intermittent
- Tay-Sachs disease
- Combined carboxylase/Biotinidase deficiency
- Cytochrome C Oxidase Deficiency/COX Complex Defect
- French-Canadian type COX mitochondrial defect
- Isovaleric acidemia
- Molybdenum cofactor deficency
- Phenylketonuria/PKU
- Pyruvate carboxylase enzyme deficiency/PCD
- Pyruvate Dehydrogenase Complex Deficiency/PDCD
- Infantile mitochondrial myopathy/Cox defect
- Pyridoxine dependency
- Beta-alaninemia
- Cerebral lipidosis disorder
- Hyperglycinemia, nonketotic
- Krebs cycle/EM cycle metabolic disorder
- MCAD/Medium chain OH-CoA Dehydrogenase def
- Prolinemia/type II
- Proprionic acidemia/congenital
- Succinic Semialdehyde dehydrogenase Deficiency
- Aminoaciduria
- Coproporphyria, hereditary
- Hartnup disease
- Juvenile ceroid lipofuscinosis/Batten-M
- Maple syrup urine disease
- McArdle's syndrome
- Ornithine transcarbamylase (OTC) defic.
- Sandhoff disease
- Tetrahydrobiopterin deficiency/Atypical PKU
- Urea cycle/metabolic disorder
Biochemical Disorders
Deficiency Disorders
Congenital, Developmental Disorders
- Cerebral palsy
- Cerebral AV malformation
- Fetal CNS disorder
- Down's Syndrome
- Hydrocephalus, obstructive
- Hydrocephalus, communicating
- Infantile muscle spasms/Hypsarrhythmia
- Fetal anomaly
- Thymic aplasia, congenital (DiGeorges)
- Thymus hypoplasia/DiGeorge syndrome
- Dandy-Walker anomaly/syndrome
- Encephalopathy, myoclonic, infantile (Kinsbourne)
- Happy puppet syndrome/Angelman syndrome
- Cerebral gigantism of childhood (Sotos)
- Corpus callosum agenesis
- Klippel-Trenaunay syndrome
- Porencephaly
- Sturge-Weber disease
- Birth asphyxia Syndrome/Hypoxic event
- Hydrocephalus
Hereditary, Familial, Genetic Disorders
- Hereditary disorder
- Epilepsy, myoclonic progressive fam'ial
- Fragile X syndrome/X-linked retardation
- Neurofibromatosis
- Tuberous Sclerosis
- Schilder disease/Adrenoleukodystrophy
- MELAS Encephalopathy
- Pallister W Syndrome
- Alpers cerebral degeneration of infancy
- Encephalomyelopathy/necro/subact/Leigh
- Hereditary mitochondrial disorder
- Hermann's syndrome
- Incontinentia pigmenti/hereditary
- Menkes steely hair disease
- Smith-Lemli-Opitz syndrome
- Genetic Disorders
Anatomic, Foreign Body, Structural Disorders
Arteriosclerotic, Vascular, Venous Disorders
Vegetative, Autonomic, Endocrine Disorders
Reference to Organ System
Pathophysiologic
Heirarchical Major Groups
Drugs
Poisoning (Specific Agent)
External Links Related to Infant Seizures
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