Disease Comparison Results (show all mode) for Factor X deficiency (Stuart-Power factor) and Dominant SCA/Spinal Cerebellar ataxias

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Dominant SCA/Spinal Cerebellar ataxias

Found: 223 | Differences: 216

Factor X deficiency (Stuart-Power factor)

Found: 25 | Differences: 18

Factor X deficiency (Stuart-Power factor) and Dominant SCA/Spinal Cerebellar ataxias sharing 7 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Hyperextensable Joints Infant
Breast Swelling Bilateral
Cardiomegaly/Heart dilatation
Tongue Protrudes Infant
Central hypotonia, infants
Delay Sitting Unsupported Infant
Distal leg weakness
Distal Muscle Weakness
Hypertonia
Mouth Hangs Open Infant
Muscles Soft/Doughy Infant
Rolling Over Delay Infant
Weakness, legs, bilateral
Absent deep tendon reflexes
Absent knee reflexes
Ankle reflexes absent
Areflexia
Ataxia
Ataxia, Cerebellar type
Ataxia/Motor tremor type
Ataxia/Posterior columns
Awkward Uncoordinated Child
Axial dystonia
Babinski's upgoing toes/bilateral
Babkin infant sign/Abnormal
Basal ganglion signs
Broad based/wide gait
Cerebellar movement disorder/signs
Cerebellar signs
Clumsiness/poor coordination
CNS symptoms/signs
Coordination/signs
Delayed speech/language development
Delayed walking milestone/child
Development Motor Skills (Milestones) Delayed
Developmental milestones delayed
Dysarthria
Dysdiadochokinesia/Alternating failure
Dyspraxic/Cerebellar speech
Dystonia
Executive function loss/apathy/inertia
Extrapyramidal signs
Fine-motor coordination problems
Finger to nose test abnormality
Gait disturbance/abnormality
Galant Infant reflex/Abnormal
Hand tremors
Head Neck Floppy Infant Hypotonia Sign
Head tremor/coarse
Infant Head Support Delay
Legs increased tone/spastic/hyperreflexic
Limb Ataxia
Limb ataxia/clumsiness child
Long tract signs
Loss of pain of temperature sensation
Loss position sense/postural sense
Mental Slowing Deteriation
Moro reflex Poor/Absent Infant
Movement or gait disorder/signs
Neurologic manifestations/signs
Neurological symptoms/signs
Nystagmus
Nystagmus, pendular
Nystagmus/Ocular dysmetria
Odd body posturing
Palmar Grasp infant Reflex Abnormal
Poor coordination legs/feet
Position sense decreased/proprioception
Position sense decreased/proprioception Legs
Primitive infant reflexes/Abnormal
Progressive neurological disorder/signs
Rooting infant sign/Abnormal
Scanning speech
Seizures
Sensory Ataxia
Slow Motor Development
Slow speech
Speech Locution Problems
Staggering Gait
Swimming infant reflex/Abnormal
Titubation Cerebellar Stagger/Nodding tremor
Tonic Neck Infant reflex/Abnormal
Tremor
Tremor in Elderly
Tremor,coarse
Truncal ataxia
Unable to tandem walk/straight line
Unsteadiness movement/Gait in a child
Vibratory sense decreased
Weak lower extremities
Shallow Breathing Infant
Difficulty Talking
Balance problems
Falling
Unable to walk/night
Walking difficulties
Weakness
True Vertigo Sign Confirmed
Clinical Presentation & Variations
Presentation/Congestive heart failure Child
Presentation/Progressive dementia Child Infant
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Life-span decreased
Onset/Young adult
Prognosis/Death about age 50 avg
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Young Adult
Family History
Family history/Parental consanguinity
Family history/Ataxia
Family history/Gait disorders
Family history/Tremor
Sex & Age Groups
Population/Adult/all
Population/Child
Population/Children/all
Population/Young adult
Laboratory Tests
Abnormal Lab Findings (Non Measured)
DNATest specific/genetics laboratory/abnormality (Lab)
Abnormal Lab Findings
Aldolase, serum (Lab)
Pseudocholinesterase, serum (Lab)
Diagnostic Test Results
Pathology
PATH/Gliosis/Brain/CNS
EKG (ECG)
EKG/Pseudoinfarction pattern/Q Waves/atypical (ECG)
EKG/Q Waves inferior leads (ECG)
EKG/Conduction defect findings (ECG)
EKG/Abnormal in children
CT Scan
CT Scan/Head Brain/cerebellar atrophy
CT Scan/Head pontine lesion
MRI/Head Cerebellar atrophy
X-RAY
Xray/Congestive heart failure signs/Chest
Xray/Large heart shadow/Chest
Xray/Chest/Lung fields/Abnormal
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Alcoholic cerebellar degeneration
Friedreich's Ataxia
Parkinsons disease
Vitamin E deficiency
Associated Disease & Complications - Causes
Ataxic neuropathy
Cardiomyopathy
Cardiomyopathy, secondary
Cerebellar ataxia
Cerebellar lesion
Cerebral palsy/ataxic type
Congenital Nystagmus
Congestive heart failure
Developmental neurologic degeneration/child
Extrapyramidal disease/manifestation
Friedreich's Ataxia
Gynecomastia
Hereditary Blindness
Kyphoscoliosis
Lateral scoliosis/Rotosclerosis
Myelopathy manifestations/involvement
Neonatal Hypotonia/Floppy Baby Syndrome
Neurodevelopmental disorders
Olivopontocerebellar degeneration
Parkinsonism, secondary
Pelizaeus-Merzbacher disease
Peripheral neuropathy
Pes cavus/High Arched Foot
Polyneuritis
REM Behavior disorder/RBD
Retinitis pigmentosa
Roussy-Levy syndrome
Scoliosis
Secondary male hypogonadism
Sensory neuropathy
Spinal cord lesion/dysfunction
Spinocerebellar ataxia, hereditary/Type I
Spinopontine atrophy/MJD disease
Heart Failure in a Child
Ataxia Disorder
Demyelinating Disease
Polyneuropathy
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Cerebellar disorder (ex)
CLASS/Neurologic (category)
CLASS/Spinal cord disorder (ex)
Pathophysiology
Pathophysiology/Frataxin gene mutation
Pathophysiology/GAA intron repeats then severe
Pathophysiology/Gene locus 9q13
Pathophysiology/Gene locus Chromosome 9
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic base pair repeats mutation
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Cerebral demyelination
Pathophysiology/CNS degeneration
Pathophysiology/Demyelination
Pathophysiology/Neurologic degenerative disorder (ex)
Pathophysiology/Posterior columns cord def
Process
PROCESS/Atrophic disorders (ex)
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Genetic expressivity variable (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Movement disorder (ex)
PROCESS/Use/Age/atrophic disorder (category)
PROCESS/Congenital CNS disorder (ex)
PROCESS/Developmental degenerative neurological disorder (ex)
PROCESS/Hereditary ataxia disorder (ex)
PROCESS/Hereditary SCA (spinocerebellar ataxias)
PROCESS/Hereditory motor/sensory neuropathy (ex)
Synonyms
Synonym
Synonym/Dejerine-Thomas atrophy
Synonym/Machado-Joseph disease
Synonym/Marie Ataxia (SCA dominant)
Synonym/MJD/Machado-Joseph disease
Synonym/Ophthalmoplegia-cerebellar ataxia syndrome
Synonym/Presenile ataxia syndrome
Synonym/SCA1 (Spinal Cerebellar Ataxia)
Synonym/SCA2 (Spinal Cerebellar Ataxia)
Synonym/SCA3 (Spinal Cerebellar Ataxia)
Synonym/SCA4 (Spinal Cerebellar Ataxia)
Synonym/SCA5 (Spinal Cerebellar Ataxia)
Synonym/SCA6 (Spinal Cerebellar Ataxia)
Synonym/SCA7 (Spinal Cerebellar Ataxia)
Synonym/SCA8 (Spinal Cerebellar Ataxia)
Synonym/Spinocerebellar ataxia, hereditary
Treatment
Other Treatments
TX/Genetic counselling
Clinical Manifestations
Signs & Symptoms
Flooding menstrual bleeding
Disease Progression
Course/Chronic disorder
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Bleeding disorders
Family history/Blood disease
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Clotting factor assay/abnormal (Lab)
Coagulation/Clotting factors decreased (Lab)
Abnormal Lab Findings - Decreased
Factor 10 (Stuart Prower) (Lab)
Abnormal Lab Findings - Increased
Clotting time/Activated clotting time test (Lab)
PIVKA II/Acarboxyprothrombin level (Lab)
Prothrombin consumption (Lab)
PT -Prothrombin time (Lab)
Thromboplastin generation time (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications
Bleeding complications/Surgery
Muscle Hematoma
Postpartum hemorrhage
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Hereditofamilial (category)
PROCESS/Coagulation derangement/disorder (ex)
Synonyms
Synonym
Synonym/Stuart-Prower factor deficiency
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