These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene. Vreeburg M; Heitink MV; Damstra RJ; Moog U; van Geel M; van Steensel MA Int J Dermatol; 2008 Nov; 47 Suppl 1():52-5. PubMed ID: 18986489 [TBL] [Abstract][Full Text] [Related]
4. Distichiasis and lymphedema: a hereditary syndrome with possible multiple defects. A report of a family. Hoover RE; Kelley JS Trans Am Ophthalmol Soc; 1971; 69():293-306. PubMed ID: 5154265 [No Abstract] [Full Text] [Related]
7. A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome. Fauret AL; Tuleja E; Jeunemaitre X; Vignes S Lymphology; 2010 Mar; 43(1):14-8. PubMed ID: 20552815 [TBL] [Abstract][Full Text] [Related]
8. Distichiasis-lymphoedema syndrome: a family report. Temple IK; Collin JR Clin Dysmorphol; 1994 Apr; 3(2):139-42. PubMed ID: 8055133 [TBL] [Abstract][Full Text] [Related]
9. Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2. Witte MH; Erickson RP; Khalil M; Dellinger M; Bernas M; Grogan T; Nitta H; Feng J; Duggan D; Witte CL Lymphology; 2009 Dec; 42(4):152-60. PubMed ID: 20218083 [TBL] [Abstract][Full Text] [Related]
10. Distichiasis-lymphedema. A hereditary syndrome of multiple congenital defects. Robinow M; Johnson GF; Verhagen AD Am J Dis Child; 1970 Apr; 119(4):343-7. PubMed ID: 5434594 [No Abstract] [Full Text] [Related]
11. Novel FOXC2 Mutation and Distichiasis in a Patient With Lymphedema-Distichiasis Syndrome. De Niear MA; Breazzano MP; Mawn LA Ophthalmic Plast Reconstr Surg; 2018; 34(3):e88-e90. PubMed ID: 29406328 [TBL] [Abstract][Full Text] [Related]
12. A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation. Fabretto A; Shardlow A; Faletra F; Lepore L; Hladnik U; Gasparini P Ophthalmic Genet; 2010 Jun; 31(2):98-100. PubMed ID: 20450314 [TBL] [Abstract][Full Text] [Related]
14. Distichiasis-lymphedema syndrome: tetralogy of Fallot, chylothorax, and neonatal death. Chen E; Larabell SK; Daniels JM; Goldstein S Am J Med Genet; 1996 Dec; 66(3):273-5. PubMed ID: 8985486 [TBL] [Abstract][Full Text] [Related]
15. [Lymphoedema distichiasis]. Marc M; Barreau M; Gerard M; Verneuil L; Derieux L; Dompmartin A Ann Dermatol Venereol; 2013 Oct; 140(10):663-5. PubMed ID: 24090902 [No Abstract] [Full Text] [Related]
16. A family with lymphoedema-distichiasis where identical twins have a discordant phenotype. Kumar S; Carver C; McCall S; Brice G; Ostergaard P; Mortimer P; Jeffery S; Clin Genet; 2007 Mar; 71(3):285-7. PubMed ID: 17309653 [No Abstract] [Full Text] [Related]
18. Phenotypic characterization of primary lymphedema. Connell F; Brice G; Mortimer P Ann N Y Acad Sci; 2008; 1131():140-6. PubMed ID: 18519967 [TBL] [Abstract][Full Text] [Related]
19. Rare association of immunoglobulin A nephropathy and lymphedema-distichiasis syndrome. Haran M; Lodha A; Rose M; Greenberg S Am J Med Sci; 2010 Mar; 339(3):288-9. PubMed ID: 20124880 [TBL] [Abstract][Full Text] [Related]
20. Distichiasis-lymphedema syndrome and the Turner phenotype. Toro-Solá MA Bol Asoc Med P R; 1991 Dec; 83(12):543-4. PubMed ID: 1811607 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]