Disease Comparison Results (show differences mode) for Olivopontocerebellar degeneration and Hereditary MVP (Flail Mitral valve)

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Hereditary MVP (Flail Mitral valve)

Found: 137 | Differences: 135

Olivopontocerebellar degeneration

Found: 63 | Differences: 61

Olivopontocerebellar degeneration and Hereditary MVP (Flail Mitral valve) sharing 2 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Hypomastia/sign
Abnormal Heart Sounds
Abnormal Heart Sounds/Child
Amyl nitrate increases murmur
Cardiac auscultation/abnormal
Cardiac Symptoms/Signs
Chest Pain
Chest Pain in Children
Chest pain, substernal/midline
Click murmur,systolic
Dizzy on Standing/Giddy Response
Ejection click/systolic
Exertional syncope/presyncope
Hand grip/decreases heart murmur
Hand grip/increases heart murmur
Heart murmur
Heart murmur/decreased supine-leg elevate
Heart 'spells'
Holosystolic murmur
Late systolic murmur
Mid-Systolic Click
Murmur,mid-diastolic
Murmur,mitral insufficiency type
Murmur/amyl nitrate increased
Murmur/decreased after PVC
Non-Pleuritic Chest Pain
Orthostatic drop in blood pressure
Palpitations/Skipped beats
Precordial Knock
Presyncope
Split S2 Heart sound
Squatting decrease/heart murmur
Standing increases systolic click
Systolic click
Systolic knock
Systolic murmur
Transient mitral insufficiency murmur
Transient/systolic murmur with chest pain
Valsalva increases heart murmur
Dizziness/Dizzy
Fatigability
Lightheadedness/giddyness/spacey
Moro Reflex unilateral Abnormal
Stroke Syndrome Child
Decreased AP diameter/chest
Dyspnea
Left anterior chest pain
Shortness of breath/SOB
Chronic/recurrent anxiety
Panic attacks
Ectomorph habitus
Enervated/extreme acute fatigue
Episodic symptoms/events
Fatigue
Fatigue Tiredness Exhaustion
Restlessness/Anxiousness
Spells/Episodes of weakness
Clinical Presentation & Variations
Presentation/Congenital Heart Disease in Adults
Demographics & Risk Factors
Past History
Past history/Heart murmur/organic
Population Group
Woman
Family History
Family history/Sudden death
Family history/Heart disease
Sex & Age Groups
Population/Female
Population/Male
Population/Woman patient
Diagnostic Test Results
EKG (ECG)
EKG/Non-specific ST-T Wave changes (ECG)
EKG/Prolonged QT interval (ECG)
EKG/Flat T Waves (ECG)
EKG/Inverted T Waves (ECG)
EKG/T Wave inversions inferior leads (ECG)
EKG/Normal (ECG)
X-RAY
Xray/Enlarged left atrium/Chest
Ultrasound
Echo/Echocardiogram Abnormal
Echo/Trans-esophageal echocardiograph/abnormal (TEE)
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Atrial myxoma
Atrial septal defect
Atrioventricular (AV) canal/congenital defect
Associated Disease & Complications - Causes
Angina pectoris
Arterial Occlusion
Atrial septal defect
Bacterial endocarditis, subacute
Cardiogenic syncope
Cerebral embolism
Cerebral vascular accident
CVA Cardiac disorders/Cause
Death/Unanticipated
Embolism
Embolism, systemic/arterial
Endocarditis, infective
Hereditary MVP (Flail Mitral valve)
Mitral regurgitation
Mitral valve prolapse syndrome
Preexcitation syndrome/ventricular
Renal embolism
Stroke /Young adult
Stroke Syndromes/Atypical causes
Stroke/Child
Subacute endocarditis, infective
Sudden death/Child
Supraventricular tachycardia
Syncope/Fainting
Transient ischemic attack/cerebral
Venticular tach/non sustained/recurrent
Ventricular ectopy/VPBs
Ventricular, paroxysmal tachycardia
Wolff-Parkinson-White syndrome
Cardiac death, sudden
Cardioembolism
Disease Mechanism & Classification
Class
CLASS/Cardiovascular (category)
CLASS/Heart disorder (ex)
CLASS/Heart valve disorder (ex)
Pathophysiology
Pathophysiology/Gene locus 16p12.1-p11.2
Pathophysiology/Gene locus Chromosome 11
Pathophysiology/Gene locus Chromosome 13
Pathophysiology/Gene locus Chromosome 16
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Cardiac embolic source
Pathophysiology/X-Linked Filamin A Gene Mutation
Process
PROCESS/Congenital/developmental (category)
PROCESS/Hereditofamilial (category)
PROCESS/Structural/anatomic/foreign body (category)
PROCESS/Vegetative-Autonomic/Endocrine (category)
PROCESS/X-Linked dominant inheritance (ex)
Synonyms
Synonym
Synonym/Mitral leaflet syndrome
Synonym/MVP
Treatment
Drug Therapy
RX/Atenolol (Tenormin)
RX/Beta-blocker
RX/Propranolol (Inderal)
RX/SBE/Antibiotic Prophylaxis
SX/Cardiac surgery
SX/Pacemaker insertion
Clinical Manifestations
Signs & Symptoms
Akinetic rigid frozen Posture
Ataxia
Athetosis
Basal ganglion signs
Cerebellar movement disorder/signs
Chorea signs
Choreoathetoid movement
Choreoathetosis
Dysdiadochokinesia/Alternating failure
Gait disturbance/abnormality
Limb Ataxia
Nystagmus
Staggering Gait
Tremor
Tremor in Elderly
Tremor,coarse
Truncal ataxia
Unsteadiness movement/Gait in a child
True Vertigo Sign Confirmed
Disease Progression
Parkinsonism plus Other CNS issues
Demographics & Risk Factors
Population Group
Aged Adult
Sex & Age Groups
Population/Adult Aged Only
Population/Adult/all
Diagnostic Test Results
CT Scan
CT Scan/Head Brain/cerebellar atrophy
MRI/Head Cerebellar atrophy
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Parkinsons disease
Associated Disease & Complications - Causes
Cerebellar ataxia
Cerebellar lesion
Congenital Nystagmus
Olivopontocerebellar degeneration
Parkinsonism, secondary
Parkinsons disease
REM Behavior disorder/RBD
Akinetic Rigid Syndrome
Ataxia Disorder
Demyelinating Disease
Disease Mechanism & Classification
Class
CLASS/Cerebellar disorder (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Cerebral demyelination
Pathophysiology/CNS degeneration
Pathophysiology/Demyelination
Pathophysiology/Neurologic degenerative disorder (ex)
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Use/Age/atrophic disorder (category)
PROCESS/Congenital CNS disorder (ex)
PROCESS/Developmental degenerative neurological disorder (ex)
PROCESS/Hereditary SCA (spinocerebellar ataxias)
Synonyms
Synonym
Synonym/Dejerine-Thomas atrophy
Synonym/Hereditary OPCA
Synonym/OPCA (Types 1,2,3,4,5)
Synonym/OPCA Fickler-Winkler type
Synonym/OPCA Holguin type (Var)
Synonym/OPCA Menzel type (Var)
Synonym/OPCA Schut-Haymaker type (Var)
Synonym/OPCA with dementia and extrapyramidal sx
Synonym/OPCA with retinal degeneration (var)
Synonym/Presenile ataxia syndrome
Synonym/SCA Cuban type (Var)
Synonym/Spinocerebellar ataxia (type 1,2,7)
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