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Absence of renal phenotype in hereditary haemorrhagic telangiectasia.
- 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.)
- Subjects :
- Adult
Arteriovenous Malformations complications
Arteriovenous Malformations genetics
Female
Genetic Testing
Humans
Kidney diagnostic imaging
Magnetic Resonance Imaging
Male
Middle Aged
Mutation genetics
Phenotype
Risk Factors
Telangiectasia, Hereditary Hemorrhagic complications
Ultrasonography
Arteriovenous Malformations diagnosis
Kidney abnormalities
Telangiectasia, Hereditary Hemorrhagic diagnosis
Telangiectasia, Hereditary Hemorrhagic genetics
Subjects
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