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

Authors

170

  1. PM
    Peter Mortimer

    St George's, University of London, United Kingdom

    6 publications · 508 citations

    6

    h-index

  2. SJ
    Steve Jeffery

    St George's, University of London, United Kingdom

    5 publications · 483 citations

    5

    h-index

  3. SM
    Sahar Mansour

    St George's, University of London, United Kingdom

    5 publications · 407 citations

    5

    h-index

  4. KG
    Kristiana Gordon

    St George's, University of London, United Kingdom

    3 publications · 207 citations

    3

    h-index

  5. FC
    Fiona Connell

    St George's, University of London, United Kingdom

    3 publications · 368 citations

    3

    h-index

1–5 of 170

Venues

  1. PubMed

    Repository · 11 publications · 405 citations

    11

    h-index

  2. Journal of the American Medical Association

    3 publications · 150 citations

    3

    h-index

  3. Journal of Medical Genetics

    JMG · 2 publications · 133 citations

    2

    h-index

  4. Acta Medica Scandinavica

    2 publications · 44 citations

    2

    h-index

  5. Prenatal Diagnosis

    2 publications · 258 citations

    2

    h-index

1–5