Milroy Disease
Milroy Disease is a hereditary form of primary lymphedema classified under lymphatic system disorders, distinguished by congenital dysfunction of the lymphatic vessels due to mutations in the FLT4 gene, leading to impaired lymphatic drainage and chronic swelling, typically in the lower limbs.
44
Publications
2.6K
Citations
170
Authors
77
Institutions
Publications per year
2017–2026
3
Variants
Hereditary Lymphedema Type IMilroy's Disease
Parents
44
A model for gene therapy of human hereditary lymphedema
Marika J. Karkkainen, Anne Saaristo, Lotta Jussila et al. · Proceedings of the National Academy of Sciences · 2001 · 611 citations · Full text
Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities
Suzanne Drury, Hywel Williams, Natalie Trump et al. · Prenatal Diagnosis · 2015 · 228 citations · Full text
Kristiana Gordon, Dörte Schulte, Glen Brice et al. · Circulation Research · 2013 · 168 citations · Full text
1–5 of 44
170
6
h-index
5
h-index
5
h-index
3
h-index
3
h-index
1–5 of 170
77
St George's, University of London
London, United Kingdom
6 h-index
46 publications
4.3K citations

Boston Children's Hospital
Boston, United States
2 h-index
8 publications
188 citations
University Hospital of Zurich
Zurich, Switzerland
2 h-index
2 publications
109 citations
University of Arizona
Tucson, United States
2 h-index
7 publications
602 citations

Lurie Children's Hospital
Chicago, United States
1 h-index
1 publications
18 citations
Hebrew University of Jerusalem
Jerusalem, Israel
1 h-index
1 publications
104 citations

The University of Queensland
Brisbane, Australia
1 h-index
7 publications
259 citations
Universidad de Londres
Mexico City, Mexico
1 h-index
7 publications
707 citations
1–8 of 77
Repository · 11 publications · 405 citations
11
h-index
3 publications · 150 citations
3
h-index
JMG · 2 publications · 133 citations
2
h-index
2 publications · 44 citations
2
h-index
2 publications · 258 citations
2
h-index
1–5