Literature DB >> 8162076

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3.

C L Shovlin1, J M Hughes, E G Tuddenham, I Temperley, Y F Perembelon, J Scott, C E Seidman, J G Seidman.   

Abstract

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant vascular disorder that is characterized by frequent nosebleeds, mucocutaneous telangiectases and vascular malformations that cause recurrent haemorrhage and arteriovenous shunting. Linkage analyses in one kindred identified an HHT locus on the long arm of chromosome 9 (maximum multipoint lod score = 6.20 between D9S60 and D9S61). Analyses in two other unrelated HHT families demonstrated that the disease in one was not linked to the locus on chromosome 9q3. We conclude that HHT is a genetically heterogeneous disorder. Based on its map location (9q3) and expression in vascular tissues, type V collagen is a possible candidate gene for HHT.

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Year:  1994        PMID: 8162076     DOI: 10.1038/ng0294-205

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  40 in total

Review 1.  Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.

Authors:  C L Shovlin; M Letarte
Journal:  Thorax       Date:  1999-08       Impact factor: 9.139

Review 2.  Pulmonary arteriovenous malformations: a clinical review.

Authors:  M Iqbal; L J Rossoff; H N Steinberg; K A Marzouk; D N Siegel
Journal:  Postgrad Med J       Date:  2000-07       Impact factor: 2.401

3.  Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1.

Authors:  A Bourdeau; U Cymerman; M E Paquet; W Meschino; W C McKinnon; A E Guttmacher; L Becker; M Letarte
Journal:  Am J Pathol       Date:  2000-03       Impact factor: 4.307

4.  A woman with an unusual case of hemoptysis.

Authors:  Narinder Pal Singh; Sameer Gulati; Sandeep Garg; Pankaj Beniwal
Journal:  CMAJ       Date:  2006-08-01       Impact factor: 8.262

5.  Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?

Authors:  J N Berg; A E Guttmacher; D A Marchuk; M E Porteous
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

6.  The value of screening for multiple arterio-venous malformations in hereditary hemorrhagic telangiectasia: a diagnostic study.

Authors:  Benedikt J Folz; Ana Cerra Wollstein; Heiko Alfke; Anja A Dünne; Burkard M Lippert; Konrad Görg; Hans-Joachim Wagner; Siegfried Bien; Jochen A Werner
Journal:  Eur Arch Otorhinolaryngol       Date:  2003-12-17       Impact factor: 2.503

7.  Visceral manifestations in hereditary haemorrhagic telangiectasia type 2.

Authors:  S A Abdalla; U W Geisthoff; D Bonneau; H Plauchu; J McDonald; S Kennedy; M E Faughnan; M Letarte
Journal:  J Med Genet       Date:  2003-07       Impact factor: 6.318

8.  Hereditary hemorrhagic telangiectasia in Japanese patients.

Authors:  Masaki Komiyama; Tomoya Ishiguro; Osamu Yamada; Hiroko Morisaki; Takayuki Morisaki
Journal:  J Hum Genet       Date:  2013-11-07       Impact factor: 3.172

9.  Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.

Authors:  P Heutink; T Haitjema; G J Breedveld; B Janssen; L A Sandkuijl; C J Bontekoe; C J Westerman; B A Oostra
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

10.  Mutation analysis of "Endoglin" and "Activin receptor-like kinase" genes in German patients with hereditary hemorrhagic telangiectasia and the value of rapid genotyping using an allele-specific PCR-technique.

Authors:  Haneen Sadick; Johanna Hage; Ulrich Goessler; Jens Stern-Straeter; Frank Riedel; Karl Hoermann; Peter Bugert
Journal:  BMC Med Genet       Date:  2009-06-09       Impact factor: 2.103

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