Disease Comparison Results (show all mode) for Hallervorden-Spatz disease (PKAN/NBIA) and Peter syndrome

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Peter syndrome

Found: 7 | Differences: 2

Hallervorden-Spatz disease (PKAN/NBIA)

Found: 63 | Differences: 58

Hallervorden-Spatz disease (PKAN/NBIA) and Peter syndrome sharing 5 common findings. (show all, show common, show differences)

Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Children/all
Associated Diseases & Rule outs
Associated Disease & Complications
Cataract
Disease Mechanism & Classification
Process
PROCESS/Eponymic (category)
PROCESS/INCIDENCE/Esoteric disease (example)
Clinical Manifestations
Signs & Symptoms
Ataxia
Athetosis
Basal ganglion signs
Choreoathetoid movement
Dysarthria
Dystonia
Gait disturbance/abnormality
Intellectual Decline Children
Mental Deficiency Child
Myoclonus/Myoclonic jerks on exam
Slow speech
Staggering Gait
Unable to tandem walk/straight line
Difficulty Talking
Cherry red spot/retinal sign
Clinical Presentation & Variations
Presentation/Mental Retardation Progressive
Presents/Myoclonus Epilepsy Mental Decline <20
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Progressive/slowly chronic illness
Onset/Childhood
Onset/gradual
Onset/insidious
Onset/Second decade
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Gait disorders
Family history/Mental retardation
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Diagnostic Test Results
Pathology
PATH/CNS/Iron deposition/Substantia Nigra region
PATH/Defective myelinatin/basal ganglia
CT Scan
MRI/Head Brain Abnormal
MRI/Head Grey matter degeneration
MRI/Head lesions basal ganglia
MRI/Head Scan Abnormal
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Gilles de Tourette syndrome
Associated Disease & Complications - Causes
Basal gangion lesion/secondary
Hallervorden-Spatz disease
Mental retardation
Ataxia Disorder
Secondary Dystonia
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Gene locus Chromosome 20
Pathophysiology/Gene PANK2 on Chromosome 20
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/CNS degeneration
Pathophysiology/Globus pallidus lesion/manifestation
Pathophysiology/Neurologic degenerative disorder (ex)
Pathophysiology/Substantia Nigra involvement/disorder (ex)
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Eponymic (category)
PROCESS/Hereditofamilial (category)
PROCESS/Hereditary ataxia disorder (ex)
PROCESS/Hereditary SCA (spinocerebellar ataxias)
Synonyms
Synonym
Synonym/Pallidal degeneration, progressive
Synonym/Pantothenate kinase 2 defect/cns
Synonym/Status dysmyelinatus
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