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Disease Comparison Results (show all mode) for Marfan's syndrome and Oromandibular facial dystonia syndrome

Clinical
Demographics
Lab
Diagnostic
Diseases
Classification
Treatment
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Found: 42 | Differences: 34

Found: 131 | Differences: 123

Marfan's syndrome and Oromandibular facial dystonia syndrome sharing 8 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Akinetic rigid frozen Posture; Facial grimacing; Facial muscle spasms; Bruxism/Teeth grinding; Muscle stiffness/rigidity; Abnormal movements/involuntary; Dysarthria; Dystonia; Extrapyramidal signs; Facial/Jaw dystonia; Forced opening/closing mouth; Gait disturbance/abnormality; Hyperkinetic Movement Disorder; Movement or gait disorder/signs; Odd body posturing; Spasms in Neck; Wry neck spasm; Difficulty Talking; Snoring
Disease Progression: Course/Chronic disorder; Course/Chronic only

Demographics & Risk Factors
Population Group: Child; Population/Pediatrics population
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all

Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs: Segawa Syndrome/Infantile Parkinsonism
Associated Disease & Complications - Causes: Dyskinesia; Dystonia muscularum deformans; Extrapyramidal disease/manifestation; Oromandibular facial dystonia syndrome; Akinetic Rigid Syndrome; Primary Dystonia

Disease Mechanism & Classification
Class: CLASS/Facial area manifestation/disorder (ex); CLASS/Muscle disorder (ex); CLASS/Neurologic (category)
Pathophysiology: Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Hereditofamilial (category); PROCESS/Hyperkinetic Movement disorders

Treatment
Drug Therapy: RX/Botulinum

Clinical Manifestations
Signs & Symptoms: Heart murmur; Right-sided parasternal AI murmur radiation; Bruising/Ecchymosis; High arched palate; Head Lag Infant Sign; Hyperextensible digits; Long arms; Long legs; Neck weakness/head nodding; Stroke Syndrome/Hereditary Disease; Decreased AP diameter/chest; Flat AP chest diameter/sign; Arms carried out from body/abducted; Arms too long for body; Cubitus valgus/sign; Genu valgus/knockneed/sign; High arches/foot/sign; Hyperextensible joints Laxity Instability; Long thin fingers/toes (arachnodactyly); Marfans thumb/little finger-wrist sign; Marfans thumb/palm sign; Pubis-heel distance/more than half height; Sternum deformities; Tall child; Tips fingers distance (span) more than height; Dysmorphic appearance/face; Ectomorph habitus; Tall Adult; Tall/thin habitus/long body/Marfanoid; Blue Sclera; Visual symptoms
Typical Clinical Presentation: Stroke syndrome kids/metabolic causes
Clinical Presentation & Variations: Presentation/Multiple deformities newborn (odd look); Presentation/Non diabetic Ketoacidosis Kids infants
Disease Progression: Course/Chronic only

Demographics & Risk Factors
Population Group: Child; Population/Pediatrics population
Family History: Family history/Aortic aneurysm; Family history/Heart disease; Family history/Skeletal malformations
Event, Activity, Behavioral & Seasonal Factors: Activity/Sports/athletic competition/contact event
Sex & Age Groups: Population/Child; Population/Children/all

Laboratory Tests
Abnormal Lab Findings (Non Measured): DNATest specific/genetics laboratory/abnormality (Lab)

Diagnostic Test Results
CT Scan: CT/Dexa-Scan Bone density Abnormal
X-RAY: Xray/Aorta/ectasia ascending/knob dilated/Chest; Xray/Chest abnormal; Xray/Chest/Lung fields/Abnormal; Xray/Long index fingers; Xray/Ribs inferior bone resorption; Xray/Ribs, notching margins

Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs: Ehlers-Danlos syndrome; Homocystinuria/homocystinemia
Associated Disease & Complications - Causes: Abdominal aortic aneurysm; Aneurysm, pulmonary artery; Aorta cystic medial necrosis/degeneration; Aorta rupture, thoracic spontaneous; Aorta, rupture, traumatic; Aortic dilatation/ectasia; Aortic regurgitation; Aortic rupture, spontaneous; Aortic stenosis, supravalvular; Atlanto/axial injury; Atlanto/odontoid dislocation/fracture; Blindness; Blindness in Children; Carotid artery dissection/aneurysm; Cataract; Cerebral vascular accident; Congenital heart disease; Death/Unanticipated; Dissecting aortic aneurysm; Flat feet/pes planus; Glaucoma; Gut Anomalies; Intestine malrotation; Kyphoscoliosis; Lateral scoliosis/Rotosclerosis; Lens dislocation; Lens dislocation, acquired; Lens subluxation; Male osteoporosis syndrome; Mitral regurgitation; Mitral valve prolapse syndrome; Myopia; Osteoporosis/osteopenia; Pathologic fractures; Pectus carinatum/pigeon chest; Pectus excavatum; Pes cavus/High Arched Foot; Pneumothorax; Pulmonic valve, regurgitation; Retina detachment; Scoliosis; Stroke /Young adult; Stroke Syndromes/Atypical causes; Stroke/Child; Sudden death/Child; Thoracic aneurysm/dilated aorta/ectasia; Thoracic Aortic Aneurysm; Valvular heart disease; Sudden Death Young Athlete; Hand anomalies; Metabolic Bone Disease

Disease Mechanism & Classification
Class: CLASS/Skeletal (category); CLASS/Connective tissue/Mesenchyme matrix disorder; CLASS/Lens involvement/disorder (ex)
Pathophysiology: Pathophysiology/Gene locus 15q21.1; Pathophysiology/Gene locus Chromosome 15; Pathophysiology/Gene Locus Identified/OMIM database; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Mutations fibrillin-1 gene/FBN1; Pathophysiology/Myxomatous degeneration heart valve; Pathophysiology/TGF-beta Signaling Vessel wall increased; Pathophysiology/Osteoporosis Secondary; Pathophysiology/Fibrillin-1 protein defect/connective tissue; Pathophysiology/Maternal Chromosome mutation; Pathophysiology/FBN1 gene
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Eponymic (category); PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Hereditary dominance/incomplete penetrance (ex).; PROCESS/Hereditofamilial (category); PROCESS/Multiple dysmorphic syndrome (ex)

Treatment
Drug Therapy: RX/Losartan (Cozaar)

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