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distichiasis-lymphoedema syndrome相关文献:
Lymphoedema-distichiasis syndrome.
Marques NS, Miranda A, Barros S, Parreira S.
BMJ Case Rep. 2016 Jan 11;2016:bcr2015213651. doi: 10.1136/bcr-2015-213651.
PMID:26759405
Lymphedema-Distichiasis Syndrome.
Mansour S, Brice GW, Jeffery S, Mortimer P.
2005 Mar 29 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:20301630
Lymphedema-distichiasis syndrome.
McDermott S, Lahiff C.
CMAJ. 2016 Feb 2;188(2):E44. doi: 10.1503/cmaj.141029. Epub 2015 Jun 29.
PMID:26124227
Distichiasis: An update on etiology, treatment and outcomes.
Singh S.
Indian J Ophthalmol. 2022 Apr;70(4):1100-1106. doi: 10.4103/ijo.IJO_1141_21.
PMID:35325995
Distichiasis-lymphoedema syndrome: a family report.
Temple IK, Collin JR.
Clin Dysmorphol. 1994 Apr;3(2):139-42.
PMID:8055133
A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.
Zhu LL, Lv YN, Chen HD, Gao XH.
Clin Exp Dermatol. 2014 Aug;39(6):731-3. doi: 10.1111/ced.12389. Epub 2014 Jul 1.
PMID:24984567
Novel mutation in the FOXC2 gene in three generations of a family with lymphoedema-distichiasis syndrome.
Sutkowska E, Gil J, Stembalska A, Hill-Bator A, Szuba A.
Gene. 2012 Apr 25;498(1):96-9. doi: 10.1016/j.gene.2012.01.098. Epub 2012 Feb 14.
PMID:22349027
Lymphoedema - distichiasis syndrome with recurrent abortions.
Sardesai VR, Mhatre MA, Patil RM.
Indian J Med Sci. 2012 May-Jun;66(5-6):141-3.
PMID:23806988
Mutations in FOXC2 in humans (lymphoedema distichiasis syndrome) cause lymphatic dysfunction on dependency.
Mellor RH, Tate N, Stanton AW, Hubert C, Mäkinen T, Smith A, Burnand KG, Jeffery S, Levick JR, Mortimer PS.
J Vasc Res. 2011;48(5):397-407. doi: 10.1159/000323484. Epub 2011 Apr 4.
PMID:21464574
Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis.
Le Collen L, Delemer B, Spodenkiewicz M, Cornillet Lefebvre P, Durand E, Vaillant E, Badreddine A, Derhourhi M, Mouhoub TA, Jouret G, Juttet P, Souchon PF, Vaxillaire M, Froguel P, Bonnefond A, Doco Fenzy M.
Orphanet J Rare Dis. 2022 Feb 28;17(1):86. doi: 10.1186/s13023-022-02248-2.
PMID:35227307
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