Mitral valve prolapse causes: Difference between revisions

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|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular'''
|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular'''


|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" |[[ST elevation myocardial infarction]], severe [[mitral annular calcification ]], ruptured [[chordae tendineae]], [[rheumatic heart disease]], [[papillary muscle dysfunction]], [[myxomatous degeneration|myxomatous]] [[mitral valve prolapse ]], [[hypertrophic cardiomyopathy]], forme fruste Barlow disease, [[Ebstein's anomaly ]], [[cardiomegaly]], [[bacterial endocarditis]], [[congenital heart disease]], [[acute myocardial ischemia]]
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" |[[Myxomatous degeneration|myxomatous]] of the [[mitral valve]], [[myocardial infarction]], severe [[mitral annular calcification]], damaged [[chordae tendineae]], [[rheumatic heart disease]], [[papillary muscle dysfunction]], [[hypertrophic cardiomyopathy]], forme fruste Barlow disease, [[Ebstein's anomaly ]], [[cardiomegaly]], [[bacterial endocarditis]], [[congenital heart disease]]


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| '''Genetic'''
| '''Genetic'''


|bgcolor="Beige"|[[Turner Syndrome]], [[spastic ataxia]], Charlevoix-Saguenay type, [[osteogenesis imperfecta]], [[Mitral valve prolapse, familial, X linked|X-linked familial mitral valve prolapse]], [[Mitral valve prolapse, familial, autosomal dominant|autosomal dominant familial mitral valve prolapse]], [[MASS phenotype]], Marfan-like syndrome  Boileau type, [[Marfan syndrome]], Hunter-Mcdonald syndrome, Furlong-Kurczynski-Hennessy syndrome
|bgcolor="Beige"|[[Turner Syndrome]], [[spastic ataxia]], Charlevoix-Saguenay type, [[osteogenesis imperfecta]], [[Mitral valve prolapse, familial, X linked|X-linked familial mitral valve prolapse]], [[Mitral valve prolapse, familial, autosomal dominant|autosomal dominant familial mitral valve prolapse]], [[MASS phenotype]], [[Marfan syndrome]], Marfan-like syndrome  Boileau type, Hunter-Mcdonald syndrome, Furlong-Kurczynski-Hennessy syndrome


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| '''Musculoskeletal/Orthopedic'''
| '''Musculoskeletal/Orthopedic'''


|bgcolor="Beige"|[[Scoliosis]], [[pectus excavatum]], dermato-cardio-skeletal syndrome Borrone type
|bgcolor="Beige"|Dermato-cardio-skeletal syndrome Borrone type


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| '''Rheumatology/Immunology/Allergy'''
| '''Rheumatology/Immunology/Allergy'''


|bgcolor="Beige"|[[SLE]], [[pseudoxanthoma elasticum]], [[polyarteritis nodosa]], [[mixed connective tissue disease]], [[Ehlers-Danlos syndrome]] type I, [[Ehlers-Danlos syndrome]] type II, [[Ehlers-Danlos syndrome]] Type V, [[connective tissue disease]]
|bgcolor="Beige"|[[SLE]], [[pseudoxanthoma elasticum]], [[polyarteritis nodosa]], [[connective tissue disease]], [[mixed connective tissue disease]], [[Ehlers-Danlos syndrome]] type I, [[Ehlers-Danlos syndrome]] type II, [[Ehlers-Danlos syndrome]] Type V


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Latest revision as of 13:43, 16 July 2013

Mitral valve prolapse Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Farman Khan, MD, MRCP [2]

Overview

Mitral valve prolapse (MVP) is a valvular heart disease that is considered to be mainly hereditary. Myxomatous degeneration of the mitral valve is a common cause of MVP. Other less common causes of MVP include connective tissue diseases such as Marfan's syndrome, Ehlers Danlos syndrome and osteogenesis imperfecta, as well as damage to the mitral valve secondary to infarction, rheumatic heart disease, hypertrophic cardiomyopathy and trauma.

Causes

Common Causes

Causes by Organ System

Cardiovascular myxomatous of the mitral valve, myocardial infarction, severe mitral annular calcification, damaged chordae tendineae, rheumatic heart disease, papillary muscle dysfunction, hypertrophic cardiomyopathy, forme fruste Barlow disease, Ebstein's anomaly , cardiomegaly, bacterial endocarditis, congenital heart disease
Chemical/Poisoning No underlying causes
Dental No underlying causes
Dermatologic No underlying causes
Drug Side Effect No underlying causes
Ear Nose Throat No underlying causes
Endocrine Graves disease
Environmental No underlying causes
Gastroenterologic No underlying causes
Genetic Turner Syndrome, spastic ataxia, Charlevoix-Saguenay type, osteogenesis imperfecta, X-linked familial mitral valve prolapse, autosomal dominant familial mitral valve prolapse, MASS phenotype, Marfan syndrome, Marfan-like syndrome Boileau type, Hunter-Mcdonald syndrome, Furlong-Kurczynski-Hennessy syndrome
Hematologic Von Willebrand disease, sickle cell disease
Iatrogenic No underlying causes
Infectious Disease Infective endocarditis, acute rheumatic fever
Musculoskeletal/Orthopedic Dermato-cardio-skeletal syndrome Borrone type
Neurologic No underlying causes
Nutritional/Metabolic Scurvy
Obstetric/Gynecologic Pregnancy
Oncologic No underlying causes
Ophthalmologic No underlying causes
Overdose/Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary No underlying causes
Renal/Electrolyte Polycystic kidney disease
Rheumatology/Immunology/Allergy SLE, pseudoxanthoma elasticum, polyarteritis nodosa, connective tissue disease, mixed connective tissue disease, Ehlers-Danlos syndrome type I, Ehlers-Danlos syndrome type II, Ehlers-Danlos syndrome Type V
Sexual No underlying causes
Trauma Trauma to mitral valve
Urologic No underlying causes
Miscellaneous Stickler Syndrome, Leopard syndrome, idiopathic, fibroelastic deficiency, Dahlberg syndrome, Beals syndrome

Causes in Alphabetical Order

References

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