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Comorbidity among HHT patients and their controls in a 20 years follow-up period

Comorbidity among HHT patients and their controls in a 20 years follow-up period

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5a0df3c75ff74c218812af0e088d9383

Comorbidity among HHT patients and their controls in a 20 years follow-up period

About this item

Full title

Comorbidity among HHT patients and their controls in a 20 years follow-up period

Publisher

England: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2018-12, Vol.13 (1), p.223-223, Article 223

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant genetic disorder with a wide variety of clinical manifestations due to the presence of multiple arteriovenous malformations in various tissues and organs.
To study the need for hospital admittance in a group of HHT patients and matched controls during a 20 years follow-up peri...

Alternative Titles

Full title

Comorbidity among HHT patients and their controls in a 20 years follow-up period

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_5a0df3c75ff74c218812af0e088d9383

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5a0df3c75ff74c218812af0e088d9383

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/s13023-018-0962-8

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