Tetralogy of fallot classification: Difference between revisions

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Created page with "__NOTOC__ {{Tetralogy of fallot}} {{CMG}}; {{AE}} {{Fs}} ==Overview== There is no established system for the classification of [disease name]. OR [Disease name] may be clas..."
 
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{{CMG}}; {{AE}} {{Fs}}
{{CMG}}; {{AE}} {{Fs}}
==Overview==
==Overview==
There is no established system for the classification of [disease name].
<br />
 
OR
 
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].
 
OR
 
[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3].
[Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].
 
OR
 
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
 
OR
 
If the staging system involves specific and characteristic findings and features:
According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
 
OR
 
The staging of [malignancy name] is based on the [staging system].
 
OR
 
There is no established system for the staging of [malignancy name].


==Classification==
==Classification==
There is no established system for the classification of [disease name].
OR


[Disease name] may be classified according to [classification method] into [number] subtypes/groups:  
[Disease name] may be classified according to [classification method] into [number] subtypes/groups:  
Line 44: Line 14:
*[Group4]
*[Group4]


OR
{|
 
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Subtypes
[Disease name] may be classified into [large number > 6] subtypes based on:
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Explanation
*[Classification method 1]
|-
*[Classification method 2]
! style="background: #DCDCDC; text-align: center;" |Acute Motor Axonal Neuropathy (AMAN)
*[Classification method 3]
| style="background: #F5F5F5;" |
 
* The most common type (85-90%).
[Disease name] may be classified into several subtypes based on:
* Prior infection can trigger it.
*[Classification method 1]
* [[Autoimmune disorder]].
*[Classification method 2]
* The target is [[schwann cell]] surface membrane or the [[myelin]].
*[Classification method 3]
* Causes [[demyelination]].
 
* In electrodiagnostic tests we can see slowing of nerve conduction.
OR
* In pathology we can see [[Lymphocyte|lymphocytic]] infiltration of peripheral nerves and [[macrophage]] invasion of [[myelin sheath]] and [[Schwann cell|schwann cells]].
 
|-
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
! style="background: #DCDCDC; text-align: center;" |Acute Motor Axonal Neuropathy (AMAN)
 
| style="background: #F5F5F5;" |
OR
* It’s common among Chinese and Japanese people.
 
* It can be triggered by C. jejuni.
'''If the staging system involves specific and characteristic findings and features:'''
* It is associated with anti[[ganglioside]] [[antibodies]].
 
* [[Autoimmunity|Autoimmune]] disorder.
According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
* Target is [[Axon|axonal]] membrane.
 
* Causes [[Axon|axonal]] degeneration in [[Motor neuron|motor neurons]].
OR
* In electrodiagnostic study we can see reduction of compound muscle [[action potential]].
 
|-
The staging of [malignancy name] is based on the [staging system].
! style="background: #DCDCDC; text-align: center;" |Acute motor and sensory axonal neuropathy
 
| style="background: #F5F5F5;" |
OR
* The incidence rate is under 10%.
* Causes [[Axon|axonal]] [[degeneration]].
* It is similar with [[Acute motor axonal neuropathy|AMAN]] but involves both motor and sensory [[Axon|axons]].
|-
! style="background: #DCDCDC; text-align: center;" |Miller Fisher syndrome
| style="background: #F5F5F5;" |
* Causes a clinical triad: [[ophthalmoplegia]], [[ataxia]] and [[areflexia]].
* Associated with [[ganglioside]] GQ1b [[antibody]].
|}


There is no established system for the staging of [malignancy name].


==References==
==References==

Revision as of 17:59, 11 February 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D.

Overview


Classification

[Disease name] may be classified according to [classification method] into [number] subtypes/groups:

  • [Group1]
  • [Group2]
  • [Group3]
  • [Group4]
Subtypes Explanation
Acute Motor Axonal Neuropathy (AMAN)
Acute Motor Axonal Neuropathy (AMAN)
Acute motor and sensory axonal neuropathy
Miller Fisher syndrome


References

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