Hypertrophic cardiomyopathy causes: Difference between revisions

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{|style="width:80%; height:100px" border="1"
{|style="width:80%; height:100px" border="1"
|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" | No underlying causes
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | [[Atrial myxoma]], [[cardiofaciocutaneous syndrome]], [[congenital generalized lipodystrophy|congenital generalized lipodystrophy type 2]], [[Costello syndrome]], [[hypertension]], [[hypertrichotic osteochondrodysplasia]], [[Noonan syndrome]], subendocardial ischemia, [[very long-chain acyl-CoA dehydrogenase deficiency]], [[Yunis-Varon syndrome]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Dermatologic'''
| '''Dermatologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Cardiofaciocutaneous syndrome]], [[congenital generalized lipodystrophy|congenital generalized lipodystrophy type 2]], [[Yunis-Varon syndrome]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Endocrine'''
| '''Endocrine'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Diabetes mellitus]], [[glycogenosis type 2]], [[thyroid disease]]
|-  
|-  
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Gastroenterologic'''
| '''Gastroenterologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Glycogenosis type 2]], [[very long-chain acyl-CoA dehydrogenase deficiency]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Genetic'''
| '''Genetic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Cardiofaciocutaneous syndrome]], [[congenital generalized lipodystrophy|congenital generalized lipodystrophy type 2]], [[Costello syndrome]], [[cytochrome c oxidase deficiency]], [[Fabry's disease]], [[familial]], [[Friedreich's ataxia]], [[gene mutation]], [[glycogenosis type 2]], [[long-chain acyl-CoA dehydrogenase deficiency]], [[malonyl-CoA decarboxylase deficiency]], [[MELAS]], [[multiple lentigines syndrome]], [[myotonic dystrophy]], [[Noonan syndrome]], sarcomeric protein mutations
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Hematologic'''
| '''Hematologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Hereditary spherocytosis]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Musculoskeletal / Ortho'''
| '''Musculoskeletal / Ortho'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Hypertrichotic osteochondrodysplasia]], [[myotonic dystrophy]], [[Yunis-Varon syndrome]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Neurologic'''
| '''Neurologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Friedreich's ataxia]], [[MELAS]], [[myotonic dystrophy]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Nutritional / Metabolic'''
| '''Nutritional / Metabolic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Cytochrome c oxidase deficiency]], dihydrolipoamide dehydrogenase deficiency, [[Fabry's disease]], [[long-chain acyl-CoA dehydrogenase deficiency]], [[malonyl-CoA decarboxylase deficiency]], [[MELAS]], [[glycogen synthase|muscle glycogen synthase deficiency]], [[very long-chain acyl-CoA dehydrogenase deficiency]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Psychiatric'''
| '''Psychiatric'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Costello syndrome]], [[hypertrichotic osteochondrodysplasia]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Miscellaneous'''
| '''Miscellaneous'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| [[Aging]], [[idiopathic]]
|-
|-
|}
|}

Revision as of 02:37, 3 November 2014

Hypertrophic Cardiomyopathy Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Hypertrophic Cardiomyopathy from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Hypertrophic cardiomyopathy causes On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Hypertrophic cardiomyopathy causes

CDC on Hypertrophic cardiomyopathy causes

Hypertrophic cardiomyopathy causes in the news

Blogs on Hypertrophic cardiomyopathy causes

Directions to Hospitals Treating Hypertrophic cardiomyopathy

Risk calculators and risk factors for Hypertrophic cardiomyopathy causes

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ogheneochuko Ajari, MB.BS, MS [2]

Overview

Hypertrophic cardiomyopathy is a condition that is most often passed down through families (inherited). It is thought to result from gene mutations that control heart muscle growth.

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Causes by Organ System

Cardiovascular Atrial myxoma, cardiofaciocutaneous syndrome, congenital generalized lipodystrophy type 2, Costello syndrome, hypertension, hypertrichotic osteochondrodysplasia, Noonan syndrome, subendocardial ischemia, very long-chain acyl-CoA dehydrogenase deficiency, Yunis-Varon syndrome
Chemical / poisoning No underlying causes
Dermatologic Cardiofaciocutaneous syndrome, congenital generalized lipodystrophy type 2, Yunis-Varon syndrome
Drug Side Effect No underlying causes
Ear Nose Throat No underlying causes
Endocrine Diabetes mellitus, glycogenosis type 2, thyroid disease
Environmental No underlying causes
Gastroenterologic Glycogenosis type 2, very long-chain acyl-CoA dehydrogenase deficiency
Genetic Cardiofaciocutaneous syndrome, congenital generalized lipodystrophy type 2, Costello syndrome, cytochrome c oxidase deficiency, Fabry's disease, familial, Friedreich's ataxia, gene mutation, glycogenosis type 2, long-chain acyl-CoA dehydrogenase deficiency, malonyl-CoA decarboxylase deficiency, MELAS, multiple lentigines syndrome, myotonic dystrophy, Noonan syndrome, sarcomeric protein mutations
Hematologic Hereditary spherocytosis
Iatrogenic No underlying causes
Infectious Disease No underlying causes
Musculoskeletal / Ortho Hypertrichotic osteochondrodysplasia, myotonic dystrophy, Yunis-Varon syndrome
Neurologic Friedreich's ataxia, MELAS, myotonic dystrophy
Nutritional / Metabolic Cytochrome c oxidase deficiency, dihydrolipoamide dehydrogenase deficiency, Fabry's disease, long-chain acyl-CoA dehydrogenase deficiency, malonyl-CoA decarboxylase deficiency, MELAS, muscle glycogen synthase deficiency, very long-chain acyl-CoA dehydrogenase deficiency
Obstetric/Gynecologic No underlying causes
Oncologic No underlying causes
Opthalmologic No underlying causes
Overdose / Toxicity No underlying causes
Psychiatric Costello syndrome, hypertrichotic osteochondrodysplasia
Pulmonary No underlying causes
Renal / Electrolyte No underlying causes
Rheum / Immune / Allergy No underlying causes
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Dental No underlying causes
Miscellaneous Aging, idiopathic

Causes in Alphabetical Order

References

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