Ataxia telangiectasia - Revision history

Michael: more

2011-08-30T04:09:30Z

← Older revision		Revision as of 04:09, 30 August 2011
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	'''Ataxia telangiectasia''', abbreviated AT, is rare autosomal recessive disorder,<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref> characterized by cerebellar pathology (ataxia) and abnormal (dilated) blood vessels (telangiectasia). It is grouped with the [[neurocutaneous syndromes]].		'''Ataxia telangiectasia''', abbreviated AT, is rare autosomal recessive disorder,<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref> characterized by cerebellar pathology (ataxia) and abnormal (dilated) blood vessels (telangiectasia). It is grouped with the [[neurocutaneous syndromes]]. Death is typically in the teens.<ref name=Ref_PCPBoD8\|679>{{Ref PCPBoD8\|679}}</ref>

	AT is characterized by:<Ref>URL: [http://www.ncbi.nlm.nih.gov/omim/208900 http://www.ncbi.nlm.nih.gov/omim/208900]. Accessed on: 3 February 2011.</ref>		AT is characterized by:<Ref>URL: [http://www.ncbi.nlm.nih.gov/omim/208900 http://www.ncbi.nlm.nih.gov/omim/208900]. Accessed on: 3 February 2011.</ref>

Michael: +micro

2011-03-31T03:42:57Z

+micro

← Older revision		Revision as of 03:42, 31 March 2011
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	*Ataxia.		*Ataxia.
	*Telangiectasias - conjunctiva, skin.<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref>		*Telangiectasias - conjunctiva, skin.<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref>

			==Microsopic==
			Features:
			*Cerebellum:<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref>
			**Loss of Purkinje cells.
			**Loss of granule cells.
			*Peripheral nerves:
			**Amphicytes - '''key feature'''.
			***Schwann cells with "bizarre" nuclear enlargement (2-5X normal).

	==References==		==References==

Michael: more

2011-03-31T03:39:34Z

← Older revision		Revision as of 03:39, 31 March 2011
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	'''Ataxia telangiectasia''', abbreviated AT, is rare ~~genetic thingy~~ characterized by cerebellar pathology (ataxia) and abnormal (dilated) blood vessels (telangiectasia). It is grouped with the [[neurocutaneous syndromes]].		'''Ataxia telangiectasia''', abbreviated AT, is rare autosomal recessive disorder,<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref> characterized by cerebellar pathology (ataxia) and abnormal (dilated) blood vessels (telangiectasia). It is grouped with the [[neurocutaneous syndromes]].

	AT is characterized by:<Ref>URL: [http://www.ncbi.nlm.nih.gov/omim/208900 http://www.ncbi.nlm.nih.gov/omim/208900]. Accessed on: 3 February 2011.</ref>		AT is characterized by:<Ref>URL: [http://www.ncbi.nlm.nih.gov/omim/208900 http://www.ncbi.nlm.nih.gov/omim/208900]. Accessed on: 3 February 2011.</ref>
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	*High propensity to develop malignancy.		*High propensity to develop malignancy.
	*Ataxia.		*Ataxia.
			*Telangiectasias - conjunctiva, skin.<ref name=Ref_PBoD8_1323>{{Ref PBoD8\|1323}}</ref>

	==References==		==References==
	{{Reflist\|1}}		{{Reflist\|2}}

	[[Category:Syndromes]]		[[Category:Syndromes]]

Michael: create a lame-o article

2011-02-03T07:49:51Z

create a lame-o article

New page

'''Ataxia telangiectasia''', abbreviated AT, is rare genetic thingy characterized by cerebellar pathology (ataxia) and abnormal (dilated) blood vessels (telangiectasia). It is grouped with the [[neurocutaneous syndromes]].

AT is characterized by:<Ref>URL: [http://www.ncbi.nlm.nih.gov/omim/208900 http://www.ncbi.nlm.nih.gov/omim/208900]. Accessed on: 3 February 2011.</ref>
*Immunodeficiency.
*High propensity to develop malignancy.
*Ataxia.

==References==
{{Reflist|1}}

[[Category:Syndromes]]