1. |
Sung HM, Chung HY, Lee SJ, et al. Clinical experience of the Klippel-Trenaunay syndrome[J].Arch Plast Surg, 2015, 42(5):552-558.DOI:10.5999/aps.2015.42.5.552.
|
2. |
Dorairaj S, Ritch R. Encephalotrigeminal angiomatosis (sturge-weber syndrome, Klippel-Trenaunay-Weber syndrome):a review[J]. Asia Pac J Ophthalmol (Phila), 2012, 1(4):226-234. DOI:10.1097/APO.0b013e31826080a9.
|
3. |
Olcaysu OO, Altun A, Olcaysu E, et al. Unilateral cataract and vitreoretinopathy in a case with klippel-trenaunay syndrome[J/OL].Case Rep Ophthalmol Med, 2014, 2014:312030[2014-06-16]. http://dx.doi.org/10.1155/2014/312030.DOI:10.1155/2014/312030.
|
4. |
Bothun ED, Kao T, Guo Y,et al. Bilateral optic nerve drusen and gliomas in Klippel-Trenaunay syndrome[J].J AAPOS, 2011, 15(1):77-79.DOI:10.1016/j.jaapos.2010.10.009.
|
5. |
Alomari AI. Persistent fetal vasculature and spontaneous hyphema in a patient with Klippel-Trenaunay-Weber syndrome[J].J AAPOS, 2010, 14(4):376. DOI:10.1016/j.jaapos.2010.06.001.
|
6. |
Abdolrahimzadeh S, Scavella V, Felli L, et al. Ophthalmic alterations in the Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis:an independent group of conditions?[J/OL]. Biomed Res Int, 2015, 2015:786519[2015-09-16]. http://dx.doi.org/10.1155/2015/786519.DOI:10.1155/2015/786519.
|