A novel mutation in the FOXC2 gene: a heterozygous insertion of adenosine (c.867insA) in a family with lymphoedema of lower limbs without distichiasis Cover

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A novel mutation in the FOXC2 gene: a heterozygous insertion of adenosine (c.867insA) in a family with lymphoedema of lower limbs without distichiasis

Radiology and Oncology

Volume 51 (2017): Issue 3 (September 2017)

By: Tanja Planinsek Rucigaj, Matija Rijavec, Jovan Miljkovic, Julij Selb and Peter Korosec

Open Access

|Jul 2017

Authors

Tanja Planinsek Rucigaj

t.rucigaj@gmail.com

Dermatovenereological Clinic, University Medical Centre Ljubljana, Ljubljana, Slovenia

Faculty of Medicine, University of Maribor, Maribor, Slovenia

Matija Rijavec

University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia

Jovan Miljkovic

Faculty of Medicine, University of Maribor, Maribor, Slovenia

Julij Selb

University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia

Peter Korosec

University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia

DOI: https://doi.org/10.1515/raon-2017-0026 | Journal eISSN: 1581-3207 | Journal ISSN: 1318-2099

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Language: English

Page range: 363 - 368

Submitted on: Dec 26, 2016

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Accepted on: May 23, 2017

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Published on: Jul 6, 2017

Published by: Association of Radiology and Oncology

In partnership with: Paradigm Publishing Services

Publication frequency: 4 issues per year

Keywords:

primary lymphedema,

FOXC2 mutation,

lower limbs lymphedema

Related subjects:

Clinical medicine,

Internal medicine,

Haematology, oncology,

© 2017 Tanja Planinsek Rucigaj, Matija Rijavec, Jovan Miljkovic, Julij Selb, Peter Korosec, published by Association of Radiology and Oncology
This work is licensed under the Creative Commons Attribution 4.0 License.

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