Ataxia telangiectasia classification: Difference between revisions
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== Classification == | == Classification == | ||
'''Ataxia-Telangiectasia''' is divided into 2 types | |||
<br>* Inherited | |||
<br>* Acquired/degenerative | |||
<br> '''Sporadic''' ataxia means there is no family history of '''A-T''' | |||
<br> '''Acquired ataxia''' is caused by degenerative diseases (eg, [[cerebellar variant of multiple systems atrophy (type C)]]), deficiency states (eg, vitamin B12, vitamin E), infections (eg, [[HIV]], [[sporadic Creutzfeldt-Jakob disease]], [[progressive multifocal leukoencephalopathy]]). | |||
<br> '''Inherited ataxia''' can be caused by X-linked, autosomal or mitochondrial inheritance.{{cite web |url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585307/}}</ref> | |||
==Overview== | ==Overview== | ||
There is no established system for the classification of [disease name]. | There is no established system for the classification of [disease name]. |
Latest revision as of 16:53, 12 June 2020
Ataxia telangiectasia Microchapters |
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Ataxia telangiectasia classification On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Classification
Ataxia-Telangiectasia is divided into 2 types
* Inherited
* Acquired/degenerative
Sporadic ataxia means there is no family history of A-T
Acquired ataxia is caused by degenerative diseases (eg, cerebellar variant of multiple systems atrophy (type C)), deficiency states (eg, vitamin B12, vitamin E), infections (eg, HIV, sporadic Creutzfeldt-Jakob disease, progressive multifocal leukoencephalopathy).
Inherited ataxia can be caused by X-linked, autosomal or mitochondrial inheritance. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585307/. Missing or empty |title=
(help)</ref>
Overview
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: [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
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:
- [Group1]
- [Group2]
- [Group3]
- [Group4]
OR
[Disease name] may be classified into [large number > 6] subtypes based on:
- [Classification method 1]
- [Classification method 2]
- [Classification method 3]
[Disease name] may be classified into several subtypes based on:
- [Classification method 1]
- [Classification method 2]
- [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].
References
So far there appear to be three forms of AT:
- Pure AT where patients present with all/most of the diagnostic symptoms.
- Attenuated AT where sufferers do not possess all of the diagnostic symptoms.
- Carrier AT where individuals with a single ATM mutation show an increased risk of cancer (known since the 1970’s).
These are sometimes classified into ‘types’ from I to IV.
- Type I is the classic syndrome with all manifestations.
- Type II lacks some of the typical findings but shows radiosensitivity.
- Type III has the classic clinical findings but is not radiosensitive.
- Type IV shows only some clinical features and is not radiosensitive.