Lymphoscintigraphic Abnormalities Associated with Milroy Disease and Lymphedema-Distichiasis Syndrome-Reference-Cited by-同舟云学术

Lymphoscintigraphic Abnormalities Associated with Milroy Disease and Lymphedema-Distichiasis Syndrome

Published:2019-12-01 Issue:6 Volume:17 Page:610-619
ISSN:1539-6851
Container-title:Lymphatic Research and Biology
language:en
Short-container-title:Lymphatic Research and Biology

Author:

Sarica Muberra¹,Gordon Kristiana¹²,van Zanten Malou¹,Heenan Susan D.³,Mortimer Peter S.¹,Irwin Andrew G.⁴,Ramachandra Vijaya⁵,Ostergaard Pia¹,Mansour Sahar¹⁵

Affiliation:

1. Molecular and Clinical Sciences, St George's University of London, London, United Kingdom.

2. Department of Dermatology, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.

3. Department of Radiology, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.

4. Department of Medical Physics and Clinical Engineering, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.

5. Department of SW Thames Regional Genetics, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.

Publisher

Mary Ann Liebert Inc

Subject

Cardiology and Cardiovascular Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/lrb.2019.0016

Reference22 articles.

1. Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis

2. Hereditary lymphedema: evidence for linkage and genetic heterogeneity

3. Mapping of Primary Congenital Lymphedema to the 5q35.3 Region

4. Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas

5. FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

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