Difference between revisions of "Hereditary hemorrhagic telangiectasia"
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*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> | *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/> | *[[Arteriovenous malformation]] = hallmark lesion.<ref name=pmid12668602/> | ||
===Diagnostic criteria=== | |||
Three of four required - Curaçao criteria:<ref>{{Cite journal | last1 = Shovlin | first1 = CL. | last2 = Guttmacher | first2 = AE. | last3 = Buscarini | first3 = E. | last4 = Faughnan | first4 = ME. | last5 = Hyland | first5 = RH. | last6 = Westermann | first6 = CJ. | last7 = Kjeldsen | first7 = AD. | last8 = Plauchu | first8 = H. | title = Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). | journal = Am J Med Genet | volume = 91 | issue = 1 | pages = 66-7 | month = Mar | year = 2000 | doi = | PMID = 10751092 }}</ref> | |||
#Epistaxes. | |||
#Telangiectasia | |||
#Visceral lesions. | |||
#Family history. | |||
==See also== | ==See also== | ||
Revision as of 14:24, 3 December 2011
Hereditary hemorrhagic telangiectasia, abbreviated HHT, is an inherited syndrome.[1] It is commonly due to a mutation in ENG (CD105).[2]
It may occur with Juvenile polyposis syndrome and be associated with a SMAD4 mutation.[3]
General (HHT1)
- Due to ENG1 mutation.
- Autosomal dominant inheritance.[4]
- Arteriovenous malformation = hallmark lesion.[4]
Diagnostic criteria
Three of four required - Curaçao criteria:[5]
- Epistaxes.
- Telangiectasia
- Visceral lesions.
- Family history.
See also
References
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 187300
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 131195
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 175050
- ↑ 4.0 4.1 Marchuk, DA.; Srinivasan, S.; Squire, TL.; Zawistowski, JS. (Apr 2003). "Vascular morphogenesis: tales of two syndromes.". Hum Mol Genet 12 Spec No 1: R97-112. PMID 12668602.
- ↑ Shovlin, CL.; Guttmacher, AE.; Buscarini, E.; Faughnan, ME.; Hyland, RH.; Westermann, CJ.; Kjeldsen, AD.; Plauchu, H. (Mar 2000). "Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).". Am J Med Genet 91 (1): 66-7. PMID 10751092.