Difference between revisions of "Hereditary hemorrhagic telangiectasia"

Jump to navigation Jump to search
more
(more)
(more)
 
Line 3: Line 3:
It may occur with [[Juvenile polyposis syndrome]] and be associated with a SMAD4 mutation.<ref>{{OMIM|175050}}</ref>
It may occur with [[Juvenile polyposis syndrome]] and be associated with a SMAD4 mutation.<ref>{{OMIM|175050}}</ref>


==General (HHT1)==
==General==
*Due to ENG1 mutation.
*Clinical diagnosis.
*Autosomal dominant inheritance.<ref name=pmid12668602>{{Cite journal  | last1 = Marchuk | first1 = DA. | last2 = Srinivasan | first2 = S. | last3 = Squire | first3 = TL. | last4 = Zawistowski | first4 = JS. | title = Vascular morphogenesis: tales of two syndromes. | journal = Hum Mol Genet | volume = 12 Spec No 1 | issue =  | pages = R97-112 | month = Apr | year = 2003 | doi =  | PMID = 12668602 }}</ref>
*[[Arteriovenous malformation]] = hallmark lesion.<ref name=pmid12668602/>


===Diagnostic criteria===
===Diagnostic criteria===
Line 14: Line 12:
#Visceral lesions.
#Visceral lesions.
#Family history.
#Family history.
===HHT1===
*Due to ''ENG1'' mutation.
*Autosomal dominant inheritance.<ref name=pmid12668602>{{Cite journal  | last1 = Marchuk | first1 = DA. | last2 = Srinivasan | first2 = S. | last3 = Squire | first3 = TL. | last4 = Zawistowski | first4 = JS. | title = Vascular morphogenesis: tales of two syndromes. | journal = Hum Mol Genet | volume = 12 Spec No 1 | issue =  | pages = R97-112 | month = Apr | year = 2003 | doi =  | PMID = 12668602 }}</ref>
*[[Arteriovenous malformation]] = hallmark lesion.<ref name=pmid12668602/>


==See also==
==See also==
48,833

edits

Navigation menu