Sturge-Weber syndrome - Revision history

Michael: wikify

2011-03-28T23:35:03Z

wikify

← Older revision		Revision as of 23:35, 28 March 2011
Line 3:		Line 3:
	#Leptomeningeal vascular malformations (angiomatosis).		#Leptomeningeal vascular malformations (angiomatosis).
	#*Results in intracranial calcifications.		#*Results in intracranial calcifications.
	#Vascular malformations of the choroid plexus associated with glaucoma.		#[[Vascular malformations]] of the choroid plexus associated with glaucoma.

	Associations:		Associations:

Michael: fix

2010-10-06T21:03:41Z

fix

← Older revision		Revision as of 21:03, 6 October 2010
Line 2:		Line 2:
	#Trigeminal distribution unilateral capillary malformations (''flame nevus'' or ''port-wine stain'').		#Trigeminal distribution unilateral capillary malformations (''flame nevus'' or ''port-wine stain'').
	#Leptomeningeal vascular malformations (angiomatosis).		#Leptomeningeal vascular malformations (angiomatosis).
	**Results in intracranial calcifications.		#*Results in intracranial calcifications.
	**Associated with neurologic signs.
	#Vascular malformations of the choroid plexus associated with glaucoma.		#Vascular malformations of the choroid plexus associated with glaucoma.

Michael: format

2010-10-06T21:01:38Z

format

← Older revision		Revision as of 21:01, 6 October 2010
Line 18:		Line 18:

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

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

Michael: fix

2010-10-06T21:01:27Z

fix

← Older revision		Revision as of 21:01, 6 October 2010
Line 1:		Line 1:
	'''Sturge-Weber syndrome''', also known as '''encephalotrigeminal angiomatosis''', is a congenital thingy that is characterized by the triad:<ref name=pmid20137589/><ref name=pmid7747906>{{cite journal \|author=Reich DS, Wiatrak BJ \|title=Upper airway obstruction in Sturge-Weber and Klippel-Trenaunay-Weber syndromes \|journal=Ann. Otol. Rhinol. Laryngol. \|volume=104 \|issue=5 \|pages=364–8 \|year=1995 \|month=May \|pmid=7747906 \|doi= \|url=}}</ref><ref>URL: [http://www.ncbi.nlm.nih.gov/omim/185300 http://www.ncbi.nlm.nih.gov/omim/185300]. Accessed on: 6 October 2010.</ref>		'''Sturge-Weber syndrome''', also known as '''encephalotrigeminal angiomatosis''', is a congenital thingy that is characterized by the triad:<ref name=pmid20137589/><ref name=pmid7747906>{{cite journal \|author=Reich DS, Wiatrak BJ \|title=Upper airway obstruction in Sturge-Weber and Klippel-Trenaunay-Weber syndromes \|journal=Ann. Otol. Rhinol. Laryngol. \|volume=104 \|issue=5 \|pages=364–8 \|year=1995 \|month=May \|pmid=7747906 \|doi= \|url=}}</ref><ref>URL: [http://www.ncbi.nlm.nih.gov/omim/185300 http://www.ncbi.nlm.nih.gov/omim/185300]. Accessed on: 6 October 2010.</ref>
	#Trigeminal distribution unilateral capillary malformations (flame nevus).		#Trigeminal distribution unilateral capillary malformations (''flame nevus'' or ''port-wine stain'').
	#Leptomeningeal vascular malformations (~~agniomatosis~~) ~~resulting~~ in intracranial calcifications ~~and~~ neurologic signs.		#Leptomeningeal vascular malformations (angiomatosis).
	#Vascular malformations of the choroid plexus ~~+/-~~ glaucoma.		**Results in intracranial calcifications.
			**Associated with neurologic signs.
			#Vascular malformations of the choroid plexus associated with glaucoma.

	Associations:		Associations:
Line 11:		Line 13:
	==Prevalence==		==Prevalence==
	*1 in 50 000 live births.<ref name=pmid20137589>{{cite journal \|author=Zhou J, Li NY, Zhou XJ, Wang JD, Ma HH, Zhang RS \|title=Sturge-Weber syndrome: a case report and review of literatures \|journal=Chin. Med. J. \|volume=123 \|issue=1 \|pages=117–21 \|year=2010 \|month=January \|pmid=20137589 \|doi= \|url=http://www.cmj.org/Periodical/paperlist.asp?id=LW20101560192150671.&linkintype=pubmed}}</ref>		*1 in 50 000 live births.<ref name=pmid20137589>{{cite journal \|author=Zhou J, Li NY, Zhou XJ, Wang JD, Ma HH, Zhang RS \|title=Sturge-Weber syndrome: a case report and review of literatures \|journal=Chin. Med. J. \|volume=123 \|issue=1 \|pages=117–21 \|year=2010 \|month=January \|pmid=20137589 \|doi= \|url=http://www.cmj.org/Periodical/paperlist.asp?id=LW20101560192150671.&linkintype=pubmed}}</ref>


	==See also==		==See also==

Michael: create

2010-10-06T20:58:57Z

create

New page

'''Sturge-Weber syndrome''', also known as '''encephalotrigeminal angiomatosis''', is a congenital thingy that is characterized by the triad:<ref name=pmid20137589/><ref name=pmid7747906>{{cite journal |author=Reich DS, Wiatrak BJ |title=Upper airway obstruction in Sturge-Weber and Klippel-Trenaunay-Weber syndromes |journal=Ann. Otol. Rhinol. Laryngol. |volume=104 |issue=5 |pages=364–8 |year=1995 |month=May |pmid=7747906 |doi= |url=}}</ref><ref>URL: [http://www.ncbi.nlm.nih.gov/omim/185300 http://www.ncbi.nlm.nih.gov/omim/185300]. Accessed on: 6 October 2010.</ref>
#Trigeminal distribution unilateral capillary malformations (flame nevus).
#Leptomeningeal vascular malformations (agniomatosis) resulting in intracranial calcifications and neurologic signs.
#Vascular malformations of the choroid plexus +/- glaucoma.

Associations:
*Intractable seizures.
*Mental retardation.
*Recurrent stroke-like episodes.

==Prevalence==
*1 in 50 000 live births.<ref name=pmid20137589>{{cite journal |author=Zhou J, Li NY, Zhou XJ, Wang JD, Ma HH, Zhang RS |title=Sturge-Weber syndrome: a case report and review of literatures |journal=Chin. Med. J. |volume=123 |issue=1 |pages=117–21 |year=2010 |month=January |pmid=20137589 |doi= |url=http://www.cmj.org/Periodical/paperlist.asp?id=LW20101560192150671.&linkintype=pubmed}}</ref>

==See also==
*[[Neurocutaneous syndromes]].

==References==
{{reflist|1}}

[[Category:Syndromes]]