Milroy Disease / Posted 3 years ago

Analysis of genes and their functions in patients with primary lymphoedema

The aim of this study is to Identify new genes linked with unexplained lymphoedema

  • Inclusion Criteria :
    • Patients with Milroy disease (lymphoedema that is confined to the lower limbs, is congenital in onset, have a family history of the disorder, and there are no associated abnormalities)
    • ‘Milroy-like’ lymphoedema but do not fit the above criteria, e.g. they may be sporadic, have onset in childhood, have slight oedema elsewhere on the body (such as a hand or part of the face)
  • Study start date : 01/09/2006
  • Study end date : 01/03/2023
  • Principal Investigator : Uruj Anjum

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