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

Clinical
Demographics
Diagnostic
Diseases
Classification
Synonyms
Treatment
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Found: 137 | Differences: 135

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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