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Differential Diagnosis For Stroke Syndrome Child
- Trauma Causes
Head trauma
Penetrating head trauma
Shaken Baby Syndrome
Traumatic Brain Hemorrhagic Necrosis- Surgical, Procedure Complication
Prosthetic heart valve dehiscence
Aortic valve prosthesis/failure
Heart valve prosthesis- Infectious Disorders (Specific Agent)
Bacterial endocarditis, subacute
Encephalitis, viral
Meningitis Bacterial
Bacterial endocarditis/acute
Chickenpox encephalitis
Fungal/Candida endocarditis
Kawasaki disease- Infected organ, Abscesses
Brain abscess
Endocarditis, infective
Prosthetic heart valve/endocarditis
Abscess, subarachnoid
Empyema, subdural
Epidural abscess
Cerebral abscess/congen. cardiac anomly- Neoplastic Disorders
Leukemic meningitis
Oligodendriglioma, brain
Polycythemia vera
Brain, ependymoma
Thrombocythemia, hemorrhagic
Atrial myxoma- Allergic, Collagen, Auto-Immune Disorders
Lupus cerebritis
Takayasu's pulseless aortitis synd.
Antiphospholipid Syndrome/APLS
Polyarteritis nodosa
Catastrophic Antiphospholipid Syndrome/APLS
Behcet's Disease- Metabolic, Storage Disorders
Primary lactic acidemia/children
Mitochondrial respiratory chain defects
Fabrys disease/Angiokeratatosis (trihexose ceramide)
Ornithine Transcarbamylase (OTC) defic.
Homocystinuria/homocystinemia
Sulfite oxidase deficiency- Congenital, Developmental Disorders
Cerebral AV malformation
Atrial septal defect, ostium secundum
Mitral valve prolapse syndrome
Atrial septal defect
Atrial septal defect (ostium primum)
Sturge-Weber disease
Patent foramen ovale/intermittant- Hereditary, Familial, Genetic Disorders
Telangiectasia,hereditary hemorrhagic
Sickle cell/thalassemia disease
Hereditary coagulopathies
MoyaMoya disease
Sickle cell anemia
Factor II mutation (20210)
Familial thrombocytosis, X-linked (Chr X)
Mitochondrial myopathy/MERRF
Antithrombin III deficiency, familial
Fabry disease crisis/syndrome
MELAS Encephalopathy
Encephalomyelopathy/necro/subact/Leigh
Factor V Leiden mutation
Protein-C deficiency
Protein-S deficiency
Pseudoxanthoma elasticum
Episodic ataxia/EA-2/Hemiplegic migraine
Hereditary MVP (Flail Mitral valve)- Anatomic, Foreign Body, Structural Disorders
Acute subdural hematoma/hemorrhage
Epidural hematoma
Subdural hematoma
Paradoxical embolism- Arteriosclerotic, Vascular, Venous Disorders
Carotid artery dissection/aneurysm
Vertebrobasilar artery dissection
Aneurysm, CNS/Berry aneurysm
Carotid, fibromuscular hyperplasia- Functional, Physiologic Variant Disorders
Abuse/neglect- Vegetative, Autonomic, Endocrine Disorders
Migraine headaches/syndrome
Arrhythmias
Atrial arrhythmias
Atrial fibrillation
Migrainous stroke/ischemic injury
Migraine equivalent
Migraine, hemiplegic type
Migraine, ophthalmoplegic/ophthalmic- Reference to Organ System
Paroxysmal Nocturnal Hemoglobinuria
Thrombocytosis
Thrombotic thrombocytopenic purpura- Pathophysiologic
Hypercoagulable/thrombophilia status- Drugs
Amphetamine (Adderall) Administration/Toxicity/ingest
Dextroamphetamine (Dexedrine) Administration/Toxicity- Poisoning (Specific Agent)
Amphetamine/Speed toxidrome/Acute
Cocaine abuse/intoxication
Methamphetamine/Speed/Amphetamine chronic/abuse- Synonyms
- 0-11 years old, Child, Child (person), Child Youth, Childhood age person, Childhood age person (person), Children, Children (0-21), Stroke syndrome
- Definition
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- External Links Related to Stroke Syndrome Child
- 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)