Disorders

Milroy Disease

Synonym(s): Hereditary Lymphedema, Type I, Hereditary Lymphoedema, Type I, Milroy Congenital Lymphedema, Milroy Congenital Lymphoedema

GeneReview OMIM

Gene	Locus	Protein
FLT4	5q34-q35	Vascular endothelial growth factor receptor 3

Laboratory	Test Method	Prenatal	Carrier *
Cliniques universitaires Saint Luc, Center for Human Genetics - Brussels, Belgium	• Sequence analysis of select exons
GENETAQ, Molecular Genetics Centre - Malaga, Spain
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
St George's University of London, SW Thames Molecular Genetics Diagnostic Laboratory - London, Great Britain	• Sequence analysis of select exons

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.