Clinical and molecular characterization of patients with hereditary hemorrhagic telangiectasia: Experience from an HHT Center of Excellence. Issue 7 (26th March 2021)
- Record Type:
- Journal Article
- Title:
- Clinical and molecular characterization of patients with hereditary hemorrhagic telangiectasia: Experience from an HHT Center of Excellence. Issue 7 (26th March 2021)
- Main Title:
- Clinical and molecular characterization of patients with hereditary hemorrhagic telangiectasia: Experience from an HHT Center of Excellence
- Authors:
- Latif, Muhammad A.
Sobreira, Nara Lygia D.
Guthrie, Kelsey S.
Motaghi, Mina
Robinson, Gina M.
Shafaat, Omid
Gong, Anna J.
Weiss, Clifford R. - Abstract:
- Abstract: In this retrospective single‐center study, we evaluated whether/how pathogenic/likely pathogenic variants of three hereditary hemorrhagic telangiectasia (HHT)–associated genes ( ENG, ACVRL1, and SMAD4 ) are associated with specific clinical presentations of HHT. We also characterized the morphological features of pulmonary arteriovenous malformations (AVMs) in patients with these variants. Pathogenic or likely pathogenic variants were detected in 64 patients. Using nonparametric statistical tests, we compared the type and prevalence of specific HHT diagnostic features associated with these three variants. Pathogenic variants in these genes resulted in gene‐specific HHT clinical presentations. Epistaxis was present in 93%, 94%, and 100% of patients with ENG, ACVRL1, and SMAD4 variants, respectively ( p = 0.79). Pulmonary AVMs were more common in patients with the ENG variant ( p = 0.034) compared with other subgroups. ACVRL1 variant was associated with the lowest frequency of pulmonary AVMs ( p = 0.034) but the highest frequency of hepatic AVMs ( p = 0.015). Patients with the ACVRL1 variant did not have significantly more pancreatic AVMs compared with the other groups ( p = 0.72). ENG, ACVRL1, and SMAD4 pathogenic or likely pathogenic variants are associated with gene‐specific HHT presentations, which is consistent with results from other HHT centers.
- Is Part Of:
- American journal of medical genetics. Volume 185:Issue 7(2021)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 185:Issue 7(2021)
- Issue Display:
- Volume 185, Issue 7 (2021)
- Year:
- 2021
- Volume:
- 185
- Issue:
- 7
- Issue Sort Value:
- 2021-0185-0007-0000
- Page Start:
- 1981
- Page End:
- 1990
- Publication Date:
- 2021-03-26
- Subjects:
- arteriovenous malformation -- genetic testing -- hereditary hemorrhagic telangiectasia -- HHT pathogenic variant -- Osler–Weber–Rendu syndrome
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.62193 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26883.xml