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A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3060383232

A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

About this item

Full title

A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

Publisher

Switzerland: MDPI AG

Journal title

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5464

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Lymphedema is a disorder that leads to excessive swelling due to lymphatic insufficiency, resulting in the accumulation of protein-rich interstitial fluid. Primary lymphedema predominantly impacts the lower extremities and is frequently linked to hereditary factors. This condition is known to be associated with variants in several genes, such as FO...

Alternative Titles

Full title

A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_3060383232

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3060383232

Other Identifiers

ISSN

1422-0067,1661-6596

E-ISSN

1422-0067

DOI

10.3390/ijms25105464

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