|1.||Vikkula, M: 2 articles (06/2015 - 10/2006)|
|2.||Glover, Thomas W: 2 articles (06/2007 - 10/2004)|
|3.||Butler, Matthew G: 2 articles (06/2007 - 10/2004)|
|4.||Dagenais, Susan L: 2 articles (06/2007 - 10/2004)|
|5.||Daniel-Spiegel, Etty: 2 articles (01/2006 - 11/2005)|
|6.||Ghalamkarpour, Arash: 2 articles (01/2006 - 11/2005)|
|7.||Spiegel, Ronen: 2 articles (01/2006 - 11/2005)|
|8.||Vikkula, Miikka: 2 articles (01/2006 - 11/2005)|
|9.||Pagan, Carlos A: 1 article (07/2015)|
|10.||Pitcher, Austin A: 1 article (07/2015)|
|1.||Lymphedema (Milroy Disease)
09/01/2002 - "To the best of our knowledge, this is the first report of early prenatal diagnosis of primary congenital lymphedema via fetal ultrasonographic examination and of spontaneous resolution of lymphedema during fetal life."
06/01/2015 - "We present two unrelated patients with antenatal features of hereditary lymphedema syndrome, in whom Milroy disease was diagnosed after birth. "
03/01/2012 - "The authors describe the case of a newborn and their family with Nonne-Milroy disease (hereditary lymphedema type I), a genetic disease that is usually characterized by lymphedema, that most often affects the lower extremities or less frequently the back of the hands. "
05/01/2010 - "Milroy's primary congenital lymphedema is a non-syndromic primary lymphedema caused mainly by autosomal dominant mutations in the FLT4 (VEGFR3) gene. "
06/01/2007 - "Milroy disease, also known as primary congenital lymphedema, is a hereditary form of lymphedema with autosomal dominant inheritance. "
02/02/1985 - "[Hereditary lymphedema, a frequently unrecognized form of chronic edema; clinical study in 2 families with Meige's disease]."
07/01/2003 - "Milroy-Nonne disease (primary hereditary lymphedema) is an uncommon congenital entity with familiar history of lower limb edema as typical clinical features. "
01/01/2000 - "To describe a patient with Meige syndrome in whom we observed the coexistence of hereditary lymphedema of the lower legs, conjunctival edema and alopecia of the lateral third of the eyebrows. "
10/01/1998 - "We report a case of lymphangiosarcoma of the pubic region, supported by immunohistochemical studies, in a 42-year-old woman affected by congenital, non-hereditary lymphedema of the left genital region and homolateral lower limb. "
10/01/1998 - "The literature concerning the cases of lymphangiosarcoma arising in congenital hereditary and non-hereditary lymphedema is reviewed. "
10/01/1998 - "To our knowledge, this is the first case of lymphangiosarcoma associated with congenital non-hereditary lymphedema confined to the pubic region. "
10/01/1998 - "Lymphangiosarcoma of the pubic region: a rare complication arising in congenital non-hereditary lymphedema."
03/13/1995 - "Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications."
|4.||Hydrops Fetalis (Fetal Edema)
06/01/2015 - "Hereditary lymphedema syndrome should be considered in cases of nonimmune hydrops fetalis/fetal edema after ruling out the more common etiologies. "
01/01/2013 - "Rarely primary congenital lymphedema may be associated with severe lymphatic dysfunction resulting in hydrops fetalis. "
01/01/2013 - "Primary congenital lymphedema complicated by hydrops fetalis: a case report and review of the literature."
03/01/2012 - "Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression."
11/01/2005 - "To report a rare case of primary congenital lymphedema (PCL) presenting as hydrops fetalis. "
09/16/2005 - "We finally highlight recent important data contributing to the understanding of the role of pericytes in tumor angiogenesis, diabetic retinopathy, and hereditary lymphedema."
10/01/2004 - "Hence, the genes responsible for hereditary lymphedema are of great interest due to the potential for providing insights into the mechanisms of lymphatic development, the diagnosis, prevention and treatment of lymphedema, and lymphangiogenesis during tumor growth. "
03/13/1995 - "This tumor, usually associated with post-mastectomy lymphedema, has not been described in late-onset hereditary lymphedema. "
|1.||Congenital hereditary lymphedema
|2.||Vascular Endothelial Growth Factor Receptor-3 (Flt 4)
|4.||Lymphedema distichiasis syndrome