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Results 1 - 10 of 17 for Lymphatic malformation 2
  1. ... Tests of GJC2 PubMed GAP JUNCTION PROTEIN, GAMMA-2; GJC2 LYMPHATIC MALFORMATION 3; LMPHM3 SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44 ...
  2. ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov ... M, Jeffery S, Mortimer P. Milroy disease and the VEGFR-3 mutation phenotype. J Med Genet. 2005 Feb;42(2):98-102. doi: 10.1136/jmg.2004.024802. ...
  3. Lymphedema (Lymphatic Education & Research Network)  
    Lymphedema/Start Here ... Lymphedema ... Lymphatic Education & Research Network ... lymphedema, lymphatic system, risk of lymphedema, treatment for lymphedema ... Lymphedema ...
  4. What Are the Types of Congenital Anomalies? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    There are two main categories of congenital anomalies: structural and functional/developmental.
  5. About Congenital Anomalies From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Birth Defects/Start Here ... Birth Defects ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes of Health
  6. How Do Health Care Providers Diagnose Congenital Anomalies? Easy-to-Read From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Birth Defects/Diagnosis and Tests ... Birth Defects ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... Easy-to-Read ... From the National ...
  7. ... play its role in the formation of the lymphatic vessel epithelium. The resulting malformation of lymphatic vessels leads to lymphangiectasia, lymphedema, and ...
  8. ... drosophila Delta homolog 4 hdelta2 notch ligand delta-2 notch ligand DLL4 Tests of DLL4 PubMed DELTA- ...
  9. ... cause Hennekam syndrome, an inherited disorder resulting from malformation of the lymphatic system. Most CCBE1 gene mutations change single protein ... generalised lymphatic dysplasia. Hum Genet. 2010 Feb;127(2):231-41. doi: 10.1007/s00439-009-0766- ...
  10. ... affected individuals have fusion of the skin between two or more fingers or toes (cutaneous syndactyly).Additional ... MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal ...
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