Hypertrophic cardiomyopathy pathophysiology: Difference between revisions
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==Overview== | ==Overview== | ||
The exact pathogenesis of | The exact pathogenesis of Hypertrophic cardiomyopathy is not fully understood. | ||
OR | OR | ||
It is thought that | It is thought that Hypertrophic cardiomyopathy is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]. | ||
OR | OR | ||
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OR | OR | ||
The progression to | The progression to Hypertrophic cardiomyopathy usually involves the [molecular pathway]. | ||
OR | OR | ||
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===Pathogenesis=== | ===Pathogenesis=== | ||
*The exact pathogenesis of | *The exact pathogenesis of Hypertrophic cardiomyopathy is not completely understood. | ||
OR | OR | ||
*It is understood that | *It is understood that Hypertrophic cardiomyopathy is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]. | ||
*[Pathogen name] is usually transmitted via the [transmission route] route to the human host. | *[Pathogen name] is usually transmitted via the [transmission route] route to the human host. | ||
*Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell. | *Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell. | ||
*[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells]. | *[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells]. | ||
*The progression to | *The progression to Hypertrophic cardiomyopathy usually involves the [molecular pathway]. | ||
*The pathophysiology of [disease/malignancy] depends on the histological subtype. | *The pathophysiology of [disease/malignancy] depends on the histological subtype. | ||
==Genetics== | ==Genetics== | ||
Hypertrophic cardiomyopathy is transmitted in [mode of genetic transmission] pattern. | |||
OR | OR | ||
Genes involved in the pathogenesis of | Genes involved in the pathogenesis of Hypertrophic cardiomyopathy include: | ||
*[Gene1] | *[Gene1] | ||
*[Gene2] | *[Gene2] | ||
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OR | OR | ||
The development of | The development of Hypertrophic cardiomyopathy is the result of multiple genetic mutations such as: | ||
*[Mutation 1] | *[Mutation 1] | ||
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==Associated Conditions== | ==Associated Conditions== | ||
Conditions associated with | Conditions associated with Hypertrophic cardiomyopathy include: | ||
*[Condition 1] | *[Condition 1] | ||
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==Gross Pathology== | ==Gross Pathology== | ||
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of | On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of Hypertrophic cardiomyopathy. | ||
==Microscopic Pathology== | ==Microscopic Pathology== | ||
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of | On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of Hypertrophic cardiomyopathy. | ||
==References== | ==References== |
Revision as of 16:45, 22 November 2019
Hypertrophic Cardiomyopathy Microchapters |
Differentiating Hypertrophic Cardiomyopathy from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Hypertrophic cardiomyopathy pathophysiology On the Web |
Directions to Hospitals Treating Hypertrophic cardiomyopathy |
Risk calculators and risk factors for Hypertrophic cardiomyopathy pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
The exact pathogenesis of Hypertrophic cardiomyopathy is not fully understood.
OR
It is thought that Hypertrophic cardiomyopathy is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to Hypertrophic cardiomyopathy usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Physiology
The normal physiology of [name of process] can be understood as follows:
Pathogenesis
- The exact pathogenesis of Hypertrophic cardiomyopathy is not completely understood.
OR
- It is understood that Hypertrophic cardiomyopathy is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to Hypertrophic cardiomyopathy usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
Hypertrophic cardiomyopathy is transmitted in [mode of genetic transmission] pattern.
OR
Genes involved in the pathogenesis of Hypertrophic cardiomyopathy include:
- [Gene1]
- [Gene2]
- [Gene3]
OR
The development of Hypertrophic cardiomyopathy is the result of multiple genetic mutations such as:
- [Mutation 1]
- [Mutation 2]
- [Mutation 3]
Associated Conditions
Conditions associated with Hypertrophic cardiomyopathy include:
- [Condition 1]
- [Condition 2]
- [Condition 3]
Gross Pathology
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of Hypertrophic cardiomyopathy.
Microscopic Pathology
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of Hypertrophic cardiomyopathy.