Difference between revisions of "Ataxia telangiectasia"

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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]]
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