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Meige lymphedema is a condition that affects the normal function of the lymphatic system. The lymphatic system transports fluids and immune cells throughout the body. Meige lymphedema is characterized by the abnormal transport of lymph fluid. When this fluid builds up abnormally, it causes swelling (lymphedema). Meige lymphedema is classified as a primary lymphedema, meaning that the malfunctioning of the lymphatic system is present from birth (congenital). Meige lymphedema is one of the few primary lymphedemas that does not have any signs or symptoms affecting other parts of the body.
Individuals with Meige lymphedema usually develop swelling during puberty. The swelling typically occurs in the lower legs and feet. Some affected individuals develop a non-contagious skin infection called cellulitis, which can further damage the thin tubes that carry lymph fluid (lymphatic vessels).
The prevalence of Meige lymphedema is unknown. Collectively, the many types of primary lymphedema affect an estimated 1.15 in 100,000 people younger than 20.
For unknown reasons, this condition affects females about three times as often as males.
The cause of Meige lymphedema is unknown. The condition is thought to be genetic because it tends to run in families, and other forms of primary lymphedema have been found to have a genetic cause. Researchers have studied many genes associated with the lymphatic system; however, no specific genetic change has been found to cause the signs and symptoms of Meige lymphedema.
Meige lymphedema appears to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of an altered gene in each cell is sufficient to cause the disorder, although no genes have been associated with Meige lymphedema.
People with Meige lymphedema usually have at least one other affected family member. In most cases, an affected person has one parent with the condition. When the condition occurs in only one person in a family, the condition is described as Meige-like lymphedema.
These resources address the diagnosis or management of Meige lymphedema and may include treatment providers.
You might also find information on the diagnosis or management of Meige lymphedema in Educational resources (http://ghr.nlm.nih.gov/condition/meige-lymphedema/show/Educational+resources) and Patient support (http://ghr.nlm.nih.gov/condition/meige-lymphedema/show/Patient+support).
General information about the diagnosis (http://ghr.nlm.nih.gov/handbook/consult/diagnosis) and management (http://ghr.nlm.nih.gov/handbook/consult/treatment) of genetic conditions is available in the Handbook. Read more about genetic testing (http://ghr.nlm.nih.gov/handbook/testing), particularly the difference between clinical tests and research tests (http://ghr.nlm.nih.gov/handbook/testing/researchtesting).
To locate a healthcare provider, see How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.
You may find the following resources about Meige lymphedema helpful. These materials are written for the general public.
You may also be interested in these resources, which are designed for healthcare professionals and researchers.
For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines (http://ghr.nlm.nih.gov/ConditionNameGuide) and How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.
Ask the Genetic and Rare Diseases Information Center (http://rarediseases.info.nih.gov/gard).
autosomal ; autosomal dominant ; cell ; congenital ; gene ; infection ; inheritance ; lymph ; lymphatic system ; lymphedema ; pattern of inheritance ; prevalence ; puberty
You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://ghr.nlm.nih.gov/glossary).
The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.