Ehlers-Danlos syndrome - Revision history

Michael: format

2012-05-07T20:04:07Z

format

← Older revision		Revision as of 20:04, 7 May 2012
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	==References==		==References==
	{{reflist\|1}}		{{reflist\|2}}

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

Michael: wikify

2012-05-05T13:56:31Z

wikify

← Older revision		Revision as of 13:56, 5 May 2012
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	*Hypermobile joints.		*Hypermobile joints.
	*Ruptures of intestinal, large arteries (e.g. [[aortic dissection]]), cornea.		*Ruptures of intestinal, large arteries (e.g. [[aortic dissection]]), cornea.
	*Poor wound healing.		*Poor [[wound healing]].

	==Subtypes==		==Subtypes==

Michael: +see also

2012-02-03T02:36:31Z

+see also

← Older revision		Revision as of 02:36, 3 February 2012
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	*[[Marfan syndrome]].		*[[Marfan syndrome]].
	*[[Vascular disease]].		*[[Vascular disease]].
			*[[Connective tissue disorders]].

	==References==		==References==

Michael at 02:36, 3 February 2012

2012-02-03T02:36:13Z

← Older revision		Revision as of 02:36, 3 February 2012
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	*Hyperextensible skin.		*Hyperextensible skin.
	*Hypermobile joints.		*Hypermobile joints.
	*Ruptures of intestinal, large arteries, cornea.		*Ruptures of intestinal, large arteries (e.g. [[aortic dissection]]), cornea.
	*Poor wound healing.		*Poor wound healing.

Michael: more

2011-05-04T15:32:17Z

← Older revision		Revision as of 15:32, 4 May 2011
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	'''Ehlers-Danlos syndrome''' is a syndrome due to a genetic defect.		'''Ehlers-Danlos syndrome''' is a syndrome due to a genetic defect.

	Features:<ref name=pmid11220066>{{cite journal \|author=Jarmulowicz M, Phillips WG \|title=Vascular Ehlers-Danlos syndrome undiagnosed during life \|journal=J R Soc Med \|volume=94 \|issue=1 \|pages=28–30 \|year=2001 \|month=January \|pmid=11220066 \|pmc=1280067 \|doi= \|url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280067/pdf/11220066.pdf}}</ref>		Features:<ref name=pmid11220066>{{cite journal \|author=Jarmulowicz M, Phillips WG \|title=Vascular Ehlers-Danlos syndrome undiagnosed during life \|journal=J R Soc Med \|volume=94 \|issue=1 \|pages=28–30 \|year=2001 \|month=January \|pmid=11220066 \|pmc=1280067 \|doi= \|url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280067/pdf/11220066.pdf}}</ref><ref name=Ref_PCPBoD89>{{Ref PCPBoD8\|89}}</ref>
	*~~Atrial rupture~~.		*Hyperextensible skin.
	*~~Intestina rupture~~.		*Hypermobile joints.
	*~~Uterine rupture~~.		*Ruptures of intestinal, large arteries, cornea.
	*~~Easy bruising~~.		*Poor wound healing.
	*~~Characteristic facies~~.
			==Subtypes==
			Classification:<ref name=Ref_PCPBoD89>{{Ref PCPBoD8\|89}}</ref>
			*There are six subtypes (classical, hypermobility, vascular, kyphoscoliosis, arthrochalasia, dermatosparaxis) - based molecular defects and clinical features.
			*Two of six are autosomal recessive (kyphoscoliosis, dermatosparaxis); the others are autosomal dominant.

	==Incidence==		==Incidence==

Michael: create

2010-09-21T13:29:06Z

create

New page

'''Ehlers-Danlos syndrome''' is a syndrome due to a genetic defect.

Features:<ref name=pmid11220066>{{cite journal |author=Jarmulowicz M, Phillips WG |title=Vascular Ehlers-Danlos syndrome undiagnosed during life |journal=J R Soc Med |volume=94 |issue=1 |pages=28–30 |year=2001 |month=January |pmid=11220066 |pmc=1280067 |doi= |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280067/pdf/11220066.pdf}}</ref>
*Atrial rupture.
*Intestina rupture.
*Uterine rupture.
*Easy bruising.
*Characteristic facies.

==Incidence==
*1 in 5000.<ref name=pmid11220066>{{cite journal |author=Jarmulowicz M, Phillips WG |title=Vascular Ehlers-Danlos syndrome undiagnosed during life |journal=J R Soc Med |volume=94 |issue=1 |pages=28–30 |year=2001 |month=January |pmid=11220066 |pmc=1280067 |doi= |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280067/pdf/11220066.pdf}}</ref>

==See also==
*[[Marfan syndrome]].
*[[Vascular disease]].

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

[[Category:Syndromes]]