Disease Comparison Results (show all mode) for Alpers cerebral degeneration of infancy and Infantile neuroaxonal dystrophy

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Infantile neuroaxonal dystrophy

Found: 74 | Differences: 56

Alpers cerebral degeneration of infancy

Found: 61 | Differences: 43

Alpers cerebral degeneration of infancy and Infantile neuroaxonal dystrophy sharing 18 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Hypertonia
Weak/Weak as a kitten (symptom)
Active reflexes
Delayed speech/language development
Development Motor Skills (Milestones) Delayed
Developmental milestones delayed
Equinus Posture/Ankles
Hyperreflexia/DTRs increased
Involuntary movements
Mental Deficiency Child
Mental/motor retardation in children/signs
Nystagmus, pendular
Psychomotor regression/infant/child
Regressing neuromotor/skills child/signs
Slow Motor Development
Spasticity/Spastic gait
Weakness/Diffuse motor loss
Psychomotor retardation
Enervated/extreme acute fatigue
Walking difficulties
Weakness
Clinical Presentation & Variations
Presentation/Progressive dementia Child Infant
Presents/Myoclonus Epilepsy Mental Decline <20
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Lethal
Course/Progressive/slowly chronic illness
Onset/Age 14-18 months
Onset/gradual
Onset/Infancy
Demographics & Risk Factors
Population Group
Child
Infant
Population/Pediatrics population
Family History
Family history/Childhood CNS degenerating disease/death
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Fetal-newborn
Population/Infant
Population/Toddler
Diagnostic Test Results
Pathology
BX/Nerve biopsy/abnormal
Electrodiagnosis
EMG/NCA Low amplitude
EMG/NCS Abnormal NC Time
Nerve Conduction Study Abnormal ENG
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Walker Warburg Syndrome
Associated Disease & Complications - Causes
CNS disease/involvement
Dementia
Developmental neurologic degeneration/child
Infantile neuroaxonal dystrophy (Seitelberger)
Mental retardation
Muscular dystrophy
Neurodevelopmental disorders
Paraplegia, spastic
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Motor neuron/unit disorder (ex)
CLASS/Brain/CNS disorder (ex)
CLASS/Lower Motor Neuron disorder (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Specific lipid accumulation tissues
Pathophysiology/Axon degeneration nerve endings
Pathophysiology/Axon dystrophic swellings/spheroids distal
Pathophysiology/CNS degeneration
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Congenital/developmental (category)
PROCESS/Hereditofamilial (category)
PROCESS/Muscular dystrophy disorder (ex)
PROCESS/Congenital CNS disorder (ex)
PROCESS/Developmental degenerative neurological disorder (ex)
Synonyms
Synonym
Synonym/Co-natal Neuroaxonal dystrophy/Variant
Synonym/INAD (infantile neuronaxonal dystrophy)
Synonym/Pre-natal neuroaxonal dystrophy/Variant
Synonym/Seitelberger disease
Clinical Manifestations
Signs & Symptoms
Central Facial Paralysis
Equinus Posture/Ankles
Infant Seizures
Seizures
Seizures/Children/recurrent
Spastic paralysis/signs
Spasticity/Spastic gait
Clinical Presentation & Variations
Presentation/Progressive dementia Child Infant
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Prognosis bad/usually
Course/Progressive
Onset/1-5 years old
Onset/Infancy
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Childhood CNS degenerating disease/death
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings
Lactic acid/Lactate (Lab)
pH, arterial blood (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications
Acidosis
Acidosis, metabolic
Alpers cerebral degeneration of infancy
Ascites in Children
Chronic liver disease
Cirrhosis
Cirrhosis in childhood
Cirrhosis/complication/secondary
Cognitive/learning disability
Congenital cataracts
Convulsions (grand mal)
Dementia
Lactic acidosis
Microcephaly/oligophrenia
Poliodystrophy/congenital
Spinal cord lesion/dysfunction
Upper GI Bleeding in children
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Liver involvement/disorder (ex)
CLASS/Brain/CNS disorder (ex)
CLASS/Neurologic (category)
CLASS/Spinal cord disorder (ex)
Pathophysiology
Pathophysiology/Gene locus 15q25
Pathophysiology/Gene locus Chromosome 15
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Congenital Brain malformation
Process
PROCESS/Hereditary mitochondrial disorder (ex)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Mitochondrial disorders (ex)
Synonyms
Synonym
Synonym/Alpers Diffuse cerebral grey matter/hepatic cirrhosis
Synonym/Alpers disease variant
Synonym/Alpers Progressive infantile Poliodystrophy
Synonym/Diffuse cerebral degeneration in infancy/Alpers
Synonym/Hereditary mitochondrial disease/Alpers type
Synonym/Poliodystrophia Cerebri Progressiva
Synonym/Progressive Cerebral Poliodystrophy
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