Surgical treatment of Milroy disease
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DOI: 10.1002/jso.25583
Abstract: Milroy disease is a form of congenital primary lymphedema affecting the lower limbs. When conservative management is ineffective, surgical treatment becomes necessary. The purpose of this study was to investigate the efficacy of vascularized lymph… read more here.
Keywords: surgical treatment; treatment; milroy disease; treatment milroy ... See more keywords
[Primary lymphedema due to Milroy disease].
Sign Up to like & getrecommendations! Published in 2017 at "Anales de pediatria"
DOI: 10.1016/j.anpedi.2015.12.007
Abstract: estudio citogenético en líquido amniótico y sangre de rogenitores, con resultado positivo en líquido amniótico padre, mostrando heterocigosis de transición c.2627T>C on cambio de aminoácidos (p.Val876Ala) en el gen FLT4 el cromosoma 5. Tras el… read more here.
Keywords: milroy disease; lymphedema due; primary lymphedema; due milroy ... See more keywords
Atypical retiform hemangioendothelioma arising in a patient with Milroy disease: a case report and review of the literature
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DOI: 10.1111/cup.12844
Abstract: Retiform hemangioendothelioma (RH) is a rare vascular neoplasm with a high rate of local recurrence and low metastatic potential. We describe an unusual case of RH in a 45‐year‐old patient with Milroy disease, with a… read more here.
Keywords: patient milroy; milroy disease; retiform hemangioendothelioma; case ... See more keywords
Milroy disease with predominant preputial involvement
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DOI: 10.1111/pde.15025
Abstract: Milroy disease is a form of congenital primary lymphedema that usually affects the lower limbs. Predominant genital lymphedema in Milroy disease is uncommon and disabling. When conservative management is ineffective, surgical treatment becomes necessary. Here,… read more here.
Keywords: predominant preputial; disease; disease predominant; milroy disease ... See more keywords
Immunohistochemical Evaluation of Histological Change in a Chinese Milroy Disease Family With Venous and Skin Abnormities
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DOI: 10.3389/fgene.2019.00206
Abstract: Background: Milroy disease (MD) is rare and autosomal dominant resulting from mutations of the vascular endothelial growth factor receptor-3 (VEGFR-3 or FLT4), which leads to dysgenesis of the lymphatic system. Methods: Here we report a… read more here.
Keywords: milroy; milroy disease; family; evaluation ... See more keywords
FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease
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DOI: 10.3390/genes12101611
Abstract: This study explored mutations in the Fms-related tyrosine kinase 4/vascular endothelial growth factor receptor 3 gene (FLT4) and lymphatic defects in patients with Milroy disease (MD). Twenty-nine patients with lower limb lymphedema were enrolled. Sixteen… read more here.
Keywords: patients milroy; flt4 mutations; lymphatic aplasia; milroy disease ... See more keywords