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Molecular genetics and clinical features of Birt–Hogg–Dubé syndrome

Molecular genetics and clinical features of Birt–Hogg–Dubé syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5119524

Molecular genetics and clinical features of Birt–Hogg–Dubé syndrome

About this item

Full title

Molecular genetics and clinical features of Birt–Hogg–Dubé syndrome

Publisher

London: Nature Publishing Group UK

Journal title

Nature reviews. Urology, 2015-10, Vol.12 (10), p.558-569

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Key Points
Birt–Hogg–Dubé (BHD) syndrome is an autosomal dominant inherited renal cancer disorder that predisposes at-risk individuals to benign, cutaneous fibrofolliculomas, pulmonary cysts, spontaneous pneumothoraces and increased risk of renal neoplasia
Renal tumours that develop in the setting of BHD syndrome are most often bilateral, mul...

Alternative Titles

Full title

Molecular genetics and clinical features of Birt–Hogg–Dubé syndrome

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5119524

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5119524

Other Identifiers

ISSN

1759-4812,1759-4820

E-ISSN

1759-4820

DOI

10.1038/nrurol.2015.206

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