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Absence of renal phenotype in hereditary haemorrhagic telangiectasia.

Authors :
Healy L
Nicholls K
Gibson R
Stella D
Bogwitz M
Taylor J
Walsh M
Donaldson L
Winship I
Source :
Internal medicine journal [Intern Med J] 2018 Oct; Vol. 48 (10), pp. 1255-1257.
Publication Year :
2018

Abstract

Hereditary haemorrhagic telangiectasia is characterised by abnormal blood vessel formation, producing telangiectasia and arteriovenous malformations in multiple organs. Information regarding possible renal involvement in hereditary haemorrhagic telangiectasia is limited. This study assessed renal structure and function in 11 patients with genetically confirmed diagnosis and known arteriovenous malformations in lung, liver, gastrointestinal tract or brain. All had significant current or past epistaxis. Despite the vascularity of the kidneys, we found no evidence of renal involvement. This observation warrants further consideration.<br /> (© 2018 Royal Australasian College of Physicians.)

Details

Language :
English
ISSN :
1445-5994
Volume :
48
Issue :
10
Database :
MEDLINE
Journal :
Internal medicine journal
Publication Type :
Academic Journal
Accession number :
30288899
Full Text :
https://doi.org/10.1111/imj.14059