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2. 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]
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5. Reduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb. Bell R; Brice G; Child AH; Murday VA; Mansour S; Sandy CJ; Collin JR; Mortimer P; Callen DF; Burnand K J Med Genet; 2000 Sep; 37(9):725. PubMed ID: 11182939 [No Abstract] [Full Text] [Related]
6. Lymphedema-distichiasis syndrome and FOXC2 gene mutation. Traboulsi EI; Al-Khayer K; Matsumoto M; Kimak MA; Crowe S; Wilson SE; Finegold DN; Ferrell RE; Meisler DM Am J Ophthalmol; 2002 Oct; 134(4):592-6. PubMed ID: 12383817 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Brice G; Mansour S; Bell R; Collin JR; Child AH; Brady AF; Sarfarazi M; Burnand KG; Jeffery S; Mortimer P; Murday VA J Med Genet; 2002 Jul; 39(7):478-83. PubMed ID: 12114478 [TBL] [Abstract][Full Text] [Related]
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12. FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate. Bahuau M; Houdayer C; Tredano M; Soupre V; Couderc R; Vazquez MP Clin Genet; 2002 Dec; 62(6):470-3. PubMed ID: 12485195 [TBL] [Abstract][Full Text] [Related]
13. 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. Conjunctival edema and distichiasis in association with congenital lymphedema of the lower legs. Ramasubramanian A; Shields CL; Palamar M; Rousta ST; Shields JA Ophthalmic Plast Reconstr Surg; 2009; 25(2):148-50. PubMed ID: 19300167 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Perinatal diagnosis of a lymphoedema-distichiasis syndrome. Brice G Prenat Diagn; 2008 Feb; 28(2):167. PubMed ID: 18236429 [No Abstract] [Full Text] [Related]
17. Renal anomalies and lymphedema distichiasis syndrome. A rare association? Jones GE; Richmond AK; Navti O; Mousa HA; Abbs S; Thompson E; Mansour S; Vasudevan PC Am J Med Genet A; 2017 Aug; 173(8):2251-2256. PubMed ID: 28544699 [TBL] [Abstract][Full Text] [Related]