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Results 1 - 10 of 34 for Primary lymphedema
  1. Meige disease 
    ... lower limbs.Meige disease is classified as a primary lymphedema, which means it is a form of lymphedema ... disease is unknown. Collectively, the many types of primary lymphedema affect an estimated 1 in 100,000 people ...
    https://medlineplus.gov/genetics/condition/meige-disease - Genetics
  2. Lymphedema (Lymphatic Education & Research Network)  
    Lymphedema/Start Here ... Lymphedema ... Lymphatic Education & Research Network ... lymphedema, lymphatic system, risk of lymphedema, treatment for lymphedema ... Lymphedema ...
    https://lymphaticnetwork.org/living-with-lymphedema/lymphedema - External Health Links
  3. Lymphedema-distichiasis syndrome 
    ... MA. Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene. Int ...
    https://medlineplus.gov/.../lymphedema-distichiasis-syndrome - Genetics
  4. Lymphedema (American Cancer Society)  
    Lymphedema/Specifics ... Lymphedema ... American Cancer Society ... Lymphedema, a build-up of fluid in the tissues that causes swelling, can be caused by cancer or its ...
    https://www.cancer.org/.../side-effects/swelling/lymphedema.html - External Health Links
  5. Lymphedema: Living with swelling and stiffness | NIH MedlinePlus Magazine 
    ... for lymphedema? There are two types of lymphedema: Primary lymphedema occurs when the lymphatic system doesn’t develop ...
    https://magazine.medlineplus.gov/...ving-with-swelling-and-stiffness - MedlinePlus Magazine
  6. Milroy disease 
    ... Karkkainen MJ, Devriendt K, Alitalo K, Vikkula M. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine ... Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema. Nat ... DN. Age of onset in hereditary lymphedema. J Pediatr. 2003 Jun;142(6):704-8. ...
    https://medlineplus.gov/genetics/condition/milroy-disease - Genetics
  7. FLT4 gene 
    ... Karkkainen MJ, Devriendt K, Alitalo K, Vikkula M. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase. Am J Hum Genet. 2000 Aug;67(2):295-301. doi: 10.1086/303019. Epub 2000 ... with VEGFR-3 signalling in primary lymphoedema. Nat Genet. 2000 Jun;25(2):153- ...
    https://medlineplus.gov/genetics/gene/flt4 - Genetics
  8. FOXC2 gene 
    ... of the eye area and lymphatic vessels, the primary regions of the body affected by lymphedema-distichiasis syndrome. More About This Health Condition FKHL14 ...
    https://medlineplus.gov/genetics/gene/foxc2 - Genetics
  9. Obesity and Cancer From the National Institutes of Health (National Cancer Institute)  
    Cancer/Related Issues ... Cancer ... Obesity/Related Issues ... Obesity ... National Cancer Institute ... From the National Institutes of Health ... A fact sheet that summarizes the ...
    https://www.cancer.gov/.../risk/obesity/obesity-fact-sheet - External Health Links
  10. Hennekam syndrome 
    ... Pamukcu O, Uzum K. Variable clinical presentation in primary lymphoedema: report of two cases. Clin ... retardation (Hennekam) syndrome: a review. Am ...
    https://medlineplus.gov/genetics/condition/hennekam-syndrome - Genetics
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