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Article

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

International journal of molecular sciences - 17 May 2024

Koksharova Galina, Kokh Natalia, Gridina Maria, Khapaev Rustam, Nimaev Vadim, Fishman Veniamin

Abstract excerpt

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 FOXC2, FLT4, and SOX18. However, many cases remain unexplained,...

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Identifiers

PMID: 38791500
DOI: 10.3390/ijms25105464
PMCID: PMC11122351

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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