Cowden syndrome pathophysiology: Difference between revisions

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It is thought that [[cowden syndrome]] is the result caused by [[phosphatase]] and tensin homolog (''[[PTEN (gene)|PTEN]])'' [[gene]] [[Mutation|mutations]]. Cowden syndrome follows autosomal dominant pattern of inheritance.  
It is thought that [[cowden syndrome]] is the result caused by [[phosphatase]] and tensin homolog (''[[PTEN (gene)|PTEN]])'' [[gene]] [[Mutation|mutations]]. Cowden syndrome follows [[autosomal dominant]] pattern of inheritance.  


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==Genetics==
==Genetics==
[Disease name] is transmitted in [mode of genetic transmission] pattern.
[[Cowden syndrome]] is transmitted in [[autosomal dominant]] pattern.
 
OR


Genes involved in the pathogenesis of [disease name] include:
Genes involved in the pathogenesis of [disease name] include:

Revision as of 18:55, 18 February 2019


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]

Overview

The exact pathogenesis of [disease name] is not fully understood.

OR

It is thought that cowden syndrome is the result caused by phosphatase and tensin homolog (PTEN) gene mutations. Cowden syndrome follows autosomal dominant pattern of inheritance.

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 [disease name] 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 [disease name] is not completely understood.

OR

  • It is understood that [disease name] 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 [disease name] usually involves the [molecular pathway].
  • The pathophysiology of [disease/malignancy] depends on the histological subtype.

Genetics

Cowden syndrome is transmitted in autosomal dominant pattern.

Genes involved in the pathogenesis of [disease name] include:

  • [Gene1]
  • [Gene2]
  • [Gene3]

OR

The development of [disease name] is the result of multiple genetic mutations such as:

  • [Mutation 1]
  • [Mutation 2]
  • [Mutation 3]

Associated Conditions

Conditions associated with [disease name] include:

  • [Condition 1]
  • [Condition 2]
  • [Condition 3]

Gross Pathology

On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].

Microscopic Pathology

On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].

References

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