Disease Comparison Results (show all mode) for Cerebellar ataxia, congenital/hered. and Hand-foot-uterus syndrome (7p15-p14.2)

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Hand-foot-uterus syndrome (7p15-p14.2)

Found: 13 | Differences: 12

Cerebellar ataxia, congenital/hered.

Found: 104 | Differences: 103

Cerebellar ataxia, congenital/hered. and Hand-foot-uterus syndrome (7p15-p14.2) sharing one common finding. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Palmar Edema
Palmar Pain
Palmar Swelling
Associated Diseases & Rule outs
Associated Disease & Complications
Hand anomalies
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Fetal/conceptual products (category)
Pathophysiology
Pathophysiology/Gene locus 7p15-p14.2
Pathophysiology/Gene locus Chromosome 7
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Hereditary Multiple anomalies syndrome [EX]
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/Vegetative-Autonomic/Endocrine (category)
Clinical Manifestations
Signs & Symptoms
Hyperextensable Joints Infant
Tongue Protrudes Infant
Central hypotonia, infants
Delay Sitting Unsupported Infant
Head Lag Infant Sign
Mouth Hangs Open Infant
Muscles Soft/Doughy Infant
Neck weakness/head nodding
Rolling Over Delay Infant
Ataxia
Ataxia, Cerebellar type
Ataxia/Motor tremor type
Awkward Uncoordinated Child
Axial dystonia
Babkin infant sign/Abnormal
Cerebellar movement disorder/signs
Cerebellar signs
Clumsiness/poor coordination
Coordination/signs
Delayed speech/language development
Delayed walking milestone/child
Development Motor Skills (Milestones) Delayed
Developmental milestones delayed
Dysarthria
Dysdiadochokinesia/Alternating failure
Dystonia
Fine-motor coordination problems
Finger to nose test abnormality
Gait disturbance/abnormality
Galant Infant reflex/Abnormal
Head Neck Floppy Infant Hypotonia Sign
Infant Head Support Delay
Involuntary Leg Movement Standing
Jerky movements
Limb Ataxia
Limb ataxia/clumsiness child
Moro reflex Poor/Absent Infant
Movement or gait disorder/signs
Nystagmus
Nystagmus, pendular
Odd body posturing
Palmar Grasp infant Reflex Abnormal
Poor coordination legs/feet
Primitive infant reflexes/Abnormal
Progressive neurological disorder/signs
Rooting infant sign/Abnormal
Slow Motor Development
Slow speech
Slurred speech
Slurred speech/Chronic
Speech Locution Problems
Staggering Gait
Swimming infant reflex/Abnormal
Tonic Neck Infant reflex/Abnormal
Tremor
Tremor in Children
Tremor,coarse
Unable to tandem walk/straight line
Unsteadiness movement/Gait in a child
Shallow Breathing Infant
Difficulty Talking
Balance problems
Falling
Walking difficulties
True Vertigo Sign Confirmed
Clinical Presentation & Variations
Presentation/Ataxia in a Child Acute
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Ataxia
Family history/Childhood CNS degenerating disease/death
Family history/Gait disorders
Family history/Tremor
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Diagnostic Test Results
Electrodiagnosis
Electronystagmography Abnormal
CT Scan
CT Scan/Head Brain/cerebellar atrophy
MRI/Head Cerebellar atrophy
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Ataxia-telangiectasia
Friedreich's Ataxia
Parkinsons disease
Associated Disease & Complications - Causes
Cerebellar ataxia
Cerebral palsy/ataxic type
Neonatal Hypotonia/Floppy Baby Syndrome
Neurodevelopmental disorders
Secondary male hypogonadism
Ataxia Disorder
Disease Mechanism & Classification
Class
CLASS/Cerebellar disorder (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Neurologic degenerative disorder (ex)
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Congenital/developmental (category)
PROCESS/Hereditofamilial (category)
PROCESS/Congenital CNS disorder (ex)
PROCESS/Developmental degenerative neurological disorder (ex)
PROCESS/Hereditary ataxia disorder (ex)
PROCESS/Hereditary SCA (spinocerebellar ataxias)
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