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Primair lymfoedeem

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lymphatic dysplasia: an update from 2010 to include molecular findings. Clin Genet. 2013: 84: 303-314.

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syndrome. Eur J HumGenet. 2015: 1-7.

10. Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, WoollardWJ, et al. Mutations in GATA2 cause primary lymphedema

associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nat Genet. 2011. DOI: 10.1038/ng.923.

11. Ostergaard P, Simpson MA, Mendola A, Vasudevan P, Connell FC, Van Impel A, et al. Mutations in KIF11 Cause Autosomal-Dominant

Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy. Am J HumGenet (2012). DOI: 10.1016/j.

ajhg.2011.12.018.

12. Ozyurta A, Sevinc E, Baykan A, Arslan D, Argun M, Pamukcu O, et al. Variable clinical presentation in primary lymphoedema: report

of two cases. Clin Dysmorphol. 2014 (23): 83-87.

13. Smeltzer DM, Stickler GB, Schirger A. Primary lymphedema in children and adolescents: a follow-up study and review. Pediatrics.

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14. Van Balkom IDC, Alers M, Allason J, Bellini C, Frank U, De Jong G, et al. Lymphedema-Lymphangiectasia-Mental Retardation

(Hennekam) Syndrome: a review. Am J Med Genet. 2002. 112:412-421.

15. Van Steensel MAM, Damstra RJ, Heitink MV, Bladergroen RS, Veraart J, Steijlen PM, et al. Novel missense mutations in the FOXC2

gene alter transcriptional activity. HumMutat. 2009: 30: E1002-E1009.

16. Vinjé- Harrewijn A, Van Beek A, Haspels P. Omgaan met lymfoedeem. Bohn Stafleu& van Loghum; 2012.

17. Vreeburg M, Heitink MV, Damstra RJ, Moog U, Van Geel M, Van Steensel MAM. Lymphedema-distichiasis syndrome: a distinct type

of primary lymphedema caused by mutations in the FOXC2 gene. Int J Dermatol. 2008. 47(1):52-55.

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19. Nederlandse Vereniging voor Dermatologie en Venereologie. Richtlijn Lymfoedeem. Utrecht: Nederlandse Vereniging voor

Dermatologie en Venereologie; 2014.

Literatuurlijst

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