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Results 1 - 10 of 10 for Lymphatic malformation 4
  1. Hennekam syndrome 
    ... Am J Med Genet. 2002 Nov 1;112(4):412-21. doi: 10.1002/ajmg.10707. Citation on PubMed
    https://medlineplus.gov/genetics/condition/hennekam-syndrome - Genetics
  2. Meige disease 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov ... dysplasia: an update from 2010 to include molecular findings. Clin Genet. 2013 Oct;84(4):303-14. doi: 10.1111/cge.12173. Epub ...
    https://medlineplus.gov/genetics/condition/meige-disease - Genetics
  3. Milroy disease 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov LYMPHATIC MALFORMATION 1; LMPHM1 PubMed Brice G, Child AH, Evans ... and atypical presentations. Clin Genet. 2006 Oct;70(4):330-5. doi: 10.1111/j.1399-0004. ...
    https://medlineplus.gov/genetics/condition/milroy-disease - Genetics
  4. GJC2 gene 
    ... GJC2 PubMed GAP JUNCTION PROTEIN, GAMMA-2; GJC2 LYMPHATIC MALFORMATION 3; LMPHM3 SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44 ... doi: 10.1093/brain/awn328. Epub 2008 Dec 4. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/gjc2 - Genetics
  5. DLL4 gene 
    ... birth. More About This Health Condition AOS6 delta 4 delta ligand 4 delta-like 4 (Drosophila) delta-like 4 homolog ...
    https://medlineplus.gov/genetics/gene/dll4 - Genetics
  6. PIK3CA gene 
    ... alpha phosphatidylinositol 3-kinase, catalytic, alpha polypeptide phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform phosphatidylinositol-4,5-bisphosphate 3-kinase 110 kDa catalytic subunit ...
    https://medlineplus.gov/genetics/gene/pik3ca - Genetics
  7. FAT4 gene 
    ... cause Hennekam syndrome, an inherited disorder resulting from malformation of the lymphatic system, which consists of a network of vessels ... member 11 CDHF14 CDHR11 FAT tumor suppressor homolog 4 FAT-J fat-like cadherin protein FAT-J ...
    https://medlineplus.gov/genetics/gene/fat4 - Genetics
  8. CCBE1 gene 
    ... cause Hennekam syndrome, an inherited disorder resulting from malformation of the lymphatic system. Most CCBE1 gene mutations change single protein ... humans. Nat Genet. 2009 Dec;41(12):1272-4. doi: 10.1038/ng.484. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/ccbe1 - Genetics
  9. Klippel-Trenaunay syndrome 
    ... Am J Med Genet. 1998 Oct 2;79(4):319-26. Citation on PubMed Gloviczki P, Driscoll ... mutations in PIK3CA. J Pediatr. 2015 Apr;166(4):1048-54.e1-5. doi: 10.1016/j. ...
    https://medlineplus.gov/.../condition/klippel-trenaunay-syndrome - Genetics
  10. Megalencephaly-capillary malformation syndrome 
    ... mutations in PIK3CA. J Pediatr. 2015 Apr;166(4):1048-54.e1-5. doi: 10.1016/j. ...
    https://medlineplus.gov/...encephaly-capillary-malformation-syndrome - Genetics