Disorders


 

Milroy Disease


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

 

GeneReviewOMIM

GeneLocusProtein
FLT45q34-q35Vascular 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• Sequence analysis of the entire coding region
 
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA• Sequence analysis of the entire coding region
• Deletion/duplication analysis
 
St George's University of London, SW Thames Molecular Genetics Diagnostic Laboratory - London, UK, 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.

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