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Results 1 - 10 of 11 for Lymphatic malformation 12
  1. GJC2 gene 
    ... connexin-47 CX46.6 Cx47 gap junction alpha-12 protein gap junction gamma-2 protein gap junction protein, gamma 2, 47kDa GJA12 Tests of GJC2 PubMed GAP JUNCTION PROTEIN, GAMMA-2; GJC2 LYMPHATIC MALFORMATION 3; LMPHM3 SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44 ...
    https://medlineplus.gov/genetics/gene/gjc2 - Genetics
  2. What Are the Types of Congenital Anomalies? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Birth Defects/Specifics ... Birth Defects ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes of Health
    https://www.nichd.nih.gov/.../conditioninfo/types - External Health Links
  3. 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
    https://www.nichd.nih.gov/health/topics/congenital-anomalies/about - External Health Links
  4. 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 ...
    https://www.nichd.nih.gov/.../conditioninfo/diagnosed - External Health Links
  5. Hennekam syndrome 
    ... play its role in the formation of the lymphatic vessel epithelium. The resulting malformation of lymphatic vessels leads to lymphangiectasia, lymphedema, and ...
    https://medlineplus.gov/genetics/condition/hennekam-syndrome - Genetics
  6. CCBE1 gene 
    ... cause Hennekam syndrome, an inherited disorder resulting from malformation of the lymphatic system. Most CCBE1 gene mutations change single protein ... dysplasia in humans. Nat Genet. 2009 Dec;41(12):1272-4. doi: 10.1038/ng.484. Citation ...
    https://medlineplus.gov/genetics/gene/ccbe1 - Genetics
  7. Turner Syndrome: A Guide for Families (Turner Syndrome Society of the United States) - PDF  
    Turner Syndrome/Living With ... Turner Syndrome ... Turner Syndrome Society of the United States ... PDF
    https://media.wix.com/...8fb9de_3b42111faa254ab2b193ecb33f71e937.pdf - External Health Links
  8. Megalencephaly-capillary malformation syndrome 
    ... e1-5. doi: 10.1016/j.jpeds.2014.12.069. Epub 2015 Feb 11. Citation on PubMed ... Am J Med Genet A. 2010 Dec;152A(12):3101-6. doi: 10.1002/ajmg.a.33514. ...
    https://medlineplus.gov/...encephaly-capillary-malformation-syndrome - Genetics
  9. Klippel-Trenaunay syndrome 
    ... e1-5. doi: 10.1016/j.jpeds.2014.12.069. Epub 2015 Feb 11. Citation on PubMed ...
    https://medlineplus.gov/.../condition/klippel-trenaunay-syndrome - Genetics
  10. PIK3CA gene 
    ... e1-5. doi: 10.1016/j.jpeds.2014.12.069. Epub 2015 Feb 11. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/pik3ca - Genetics
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