Literature DB >> 29470256

Systematic screening in hereditary hemorrhagic telangiectasia: a review.

Steven Kroon1, Repke J Snijder1, Marie E Faughnan2,3, Hans-Jurgen Mager1.   

Abstract

PURPOSE OF REVIEW: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disease characterized by telangiectasia and arteriovenous malformations (AVMs). To date, five genetic types of HHT and one combined juvenile polyposis syndrome and HHT are known. Clinical and genetic screening of patients suspected with HHT is recommended to confirm the diagnosis and to prevent complications associated with HHT. The aim of this article is to give an overview of the evidence and to formulate a recommendation for clinicians concerning screening for HHT. RECENT
FINDINGS: Complications of HHT such as stroke, brain abscess and intracranial hemorrhage are caused by pulmonary and cerebral AVMs (CAVMs) and can often be prevented by screening and treatment when possible. Screening and treatment of these AVMs will result in an increased life expectancy comparable with that of the general population as opposed to unscreened and untreated HHT patients.
SUMMARY: Screening of HHT patients and their first-degree relatives is recommended to prevent severe complications including stroke, brain abscess and intracranial hemorrhage.

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Mesh:

Year:  2018        PMID: 29470256     DOI: 10.1097/MCP.0000000000000472

Source DB:  PubMed          Journal:  Curr Opin Pulm Med        ISSN: 1070-5287            Impact factor:   3.155


  6 in total

Review 1.  Recognizing genetic disease: A key aspect of pediatric pulmonary care.

Authors:  Lael M Yonker; Megan H Hawley; Peter P Moschovis; Mengdi Lu; T Bernard Kinane
Journal:  Pediatr Pulmonol       Date:  2020-07

2.  Screening in cryptogenic brain abscess: Do not forget pulmonary arteriovenous malformations.

Authors:  Jasmien Rens; Thomas Van Thielen; Aurelie Derweduwen; Koen Goedseels; Robert Hes; Lars de Jong
Journal:  Surg Neurol Int       Date:  2021-04-26

3.  Thalidomide for the Management of Bleeding Episodes in Patients with Hereditary Hemorrhagic Telangiectasia: Effects on Epistaxis Severity Score and Quality of Life

Authors:  Mehmet Baysal; Elif G. Ümit; Hakkı Onur Kırkızlar; Ali Caner Özdöver; Ahmet Muzaffer Demir
Journal:  Turk J Haematol       Date:  2018-06-08       Impact factor: 1.831

4.  Gender differences in hereditary hemorrhagic telangiectasia severity.

Authors:  J M Mora-Luján; A Iriarte; E Alba; M A Sánchez-Corral; P Cerdà; F Cruellas; Q Ordi; X Corbella; J Ribas; J Castellote; A Riera-Mestre
Journal:  Orphanet J Rare Dis       Date:  2020-03-02       Impact factor: 4.123

5.  Hereditary Hemorrhagic Telangiectasia (HHT) and Survival: The Importance of Systematic Screening and Treatment in HHT Centers of Excellence.

Authors:  Els M de Gussem; Steven Kroon; Anna E Hosman; Johannes C Kelder; Martijn C Post; Repke J Snijder; Johannes J Mager
Journal:  J Clin Med       Date:  2020-11-06       Impact factor: 4.241

6.  Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia.

Authors:  Kana Kitayama; Tomoya Ishiguro; Masaki Komiyama; Takayuki Morisaki; Hiroko Morisaki; Gaku Minase; Kohei Hamanaka; Satoko Miyatake; Naomichi Matsumoto; Masaru Kato; Toru Takahashi; Tohru Yorifuji
Journal:  BMC Med Genomics       Date:  2021-12-06       Impact factor: 3.063

  6 in total

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