Disease Comparison Results (show all mode) for Hereditary warfarin resistance and Van Bogaert encephalitis

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Van Bogaert encephalitis

Found: 74 | Differences: 65

Hereditary warfarin resistance

Found: 12 | Differences: 3

Hereditary warfarin resistance and Van Bogaert encephalitis sharing 9 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Adolescent
Altered mental status Mental status change
Delirium
Delirium/Agitated delirium
Drowsiness/somnolence
Fatigability
Gait disturbance/abnormality
Impaired judgement/signs
Irritability/short tempered
Movement or gait disorder/signs
Paralysis
Seizures
Psychiatric manifestations/problems/difficulties
Schizoid personality
Constitutional symptoms
Fatigue
Fatigue Tiredness Exhaustion
Clinical Presentation & Variations
Presentation/Acute encephalopathy Child
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Progressive
Course/Progressive/slowly chronic illness
Onset/adult
Onset/insidious
Onset/Young adult
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Young Adult
Family History
Family history/Dementia
Family history/Nerve disease
Sex & Age Groups
Population/Adolescent
Population/Adult ('twenties')
Population/Adult/all
Population/Child
Population/Children/all
Population/Young adult
Laboratory Tests
Abnormal Lab Findings
URINE Lake test/Brown metachromasia sediment
URINE Sediment brown metachromasia
Diagnostic Test Results
Other Tests & Procedures
Lumbar puncture/Increased CSF pressure/LP test
Pathology
BX/Nerve biopsy/abnormal
BX/Nerve biopsy/Brown metachromasia/Schwann cells
PATH/Brain/White matter lesion/disease
PATH/CNS/Metachromatic/galactosphingosulfatide deposits
CT Scan
MRI/Head Scan Abnormal
Associated Diseases & Rule outs
Associated Disease & Complications
CNS disease/involvement
Convulsions (grand mal)
Dementia
Encephalitis
Leukodystrophy
Leukoencephalopathy process
Paralytic Disorder
Paranoia reaction
Psychosis
Quadriparesis/quadriplegia
Van Bogaert encephalitis
Demyelinating Disease
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Primary organ/system disorder (ex)
CLASS/Brain/CNS disorder (ex)
CLASS/Cerebral cortex disorder (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/CSF Pressure Increased
Pathophysiology/Diffuse/progressive cerebral disease
Pathophysiology/Galactosphingosulfatides myelin deposits
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Degenerative/necrosis disorder (category)
PROCESS/Hereditofamilial (category)
PROCESS/Inflammatory/infection (ex)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Storage disorder (ex)
PROCESS/Use/Age/atrophic disorder (category)
PROCESS/Leukodystrophy process (ex)
Synonyms
Synonym
Synonym/Adult form/metachromatic leukodystrophy
Clinical Manifestations
Clinical Presentation & Variations
Presentation/Warfarin Insensitivity Tolerance
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Systemic/no comment (category)
Process
PROCESS/Hereditofamilial (category)
PROCESS/Metabolic/storage disorder (category)
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