272 related articles for article (PubMed ID: 27374914)
1. Phakomatosis pigmentovascularis type IIb: A case with Klippel-Trenáunay syndrome and extensive dermal melanocytosis as nevus of Ota, nevus of Ito and ectopic Mongolian spots.
Namiki T; Takahashi M; Nojima K; Ueno M; Hanafusa T; Tokoro S; Yokozeki H
J Dermatol; 2017 Mar; 44(3):e32-e33. PubMed ID: 27374914
[No Abstract] [Full Text] [Related]
2. The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.
Ma H; Liao M; Qiu S; Luo R; Lu R; Lu C
An Bras Dermatol; 2015; 90(3 Suppl 1):10-2. PubMed ID: 26312661
[TBL] [Abstract][Full Text] [Related]
3. Phakomatosis pigmentovascularis: Implications for severity with special reference to Mongolian spots associated with Sturge-Weber and Klippel-Trenaunay syndromes.
Hall BD; Cadle RG; Morrill-Cornelius SM; Bay CA
Am J Med Genet A; 2007 Dec; 143A(24):3047-53. PubMed ID: 17937434
[TBL] [Abstract][Full Text] [Related]
4. Phacomatosis pigmentovascularis type IIa--case report.
Segatto MM; Schmitt EU; Hagemann LN; Silva RC; Cattani CA
An Bras Dermatol; 2013; 88(6 Suppl 1):85-8. PubMed ID: 24346888
[TBL] [Abstract][Full Text] [Related]
5. An infantile case of Sturge-Weber syndrome in association with Klippel-Trenaunay-Weber syndrome and phakomatosis pigmentovascularis.
Lee CW; Choi DY; Oh YG; Yoon HS; Kim JD
J Korean Med Sci; 2005 Dec; 20(6):1082-4. PubMed ID: 16361829
[TBL] [Abstract][Full Text] [Related]
6. Phakomatosis pigmentovascularis type IIb.
Wang B; Yang M; Lv S; Xu N; Zhang Y; Wu S; Wang J; Li F
J Dtsch Dermatol Ges; 2019 Nov; 17(11):1179-1182. PubMed ID: 31765096
[No Abstract] [Full Text] [Related]
7. An unusual case of Sturge-Weber syndrome in association with phakomatosis pigmentovascularis and Klippel-Trenaunay-Weber syndrome.
Saricaoğlu MS; Güven D; Karakurt A; Sengun A; Ziraman I
Retina; 2002 Jun; 22(3):368-71. PubMed ID: 12055477
[No Abstract] [Full Text] [Related]
8. CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH OVERLAPPING STURGE-WEBER SYNDROME AND KLIPPEL-TRENAUNAY SYNDROME.
Fry MV; Williams BK; Kim HJ; Di Nicola M
Retin Cases Brief Rep; 2023 Mar; 17(2):130-133. PubMed ID: 33907078
[TBL] [Abstract][Full Text] [Related]
9. Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis.
Hayashi S; Kaminaga T; Tantcheva-Poor I; Hamasaki Y; Hatamochi A
J Dermatol; 2016 Feb; 43(2):225-6. PubMed ID: 26498915
[No Abstract] [Full Text] [Related]
10. Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb.
Mandal RK; Ghosh SK; Koley S; Roy AC
Indian J Dermatol Venereol Leprol; 2014; 80(1):51-3. PubMed ID: 24448125
[TBL] [Abstract][Full Text] [Related]
11. Phakomatosis pigmentovascularis and Lisch nodules. Relationship between Von Recklinghausen and phakomatosis pigmentovascularis?
Ruiz Villaverde R; Viera Ramirez A; Linares Solano J; Naranjo Sintes R; Gutierrez Salmerón MT
J Eur Acad Dermatol Venereol; 2003 Jan; 17(1):53-5. PubMed ID: 12602970
[TBL] [Abstract][Full Text] [Related]
12. Large aberrant Mongolian spots coexisting with cutis marmorata telangiectatica congenita (phacomatosis pigmentovascularis type V or phacomatosis cesiomarmorata).
Torrelo A; Zambrano A; Happle R
J Eur Acad Dermatol Venereol; 2006 Mar; 20(3):308-10. PubMed ID: 16503893
[TBL] [Abstract][Full Text] [Related]
13. Clinical characteristics and treatment of 52 cases of phakomatosis pigmentovascularis.
Shin H; Kim YG; Kim YE; Park H
J Dermatol; 2019 Oct; 46(10):843-848. PubMed ID: 31389056
[TBL] [Abstract][Full Text] [Related]
14. Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
Abdolrahimzadeh S; Scavella V; Felli L; Cruciani F; Contestabile MT; Recupero SM
Biomed Res Int; 2015; 2015():786519. PubMed ID: 26451379
[TBL] [Abstract][Full Text] [Related]
15. CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH KLIPPEL-TRENAUNAY SYNDROME.
Shields CL; Di Nicola M; Pellegrini M; Shields JA
Retina; 2018 Nov; 38(11):2220-2227. PubMed ID: 28937525
[TBL] [Abstract][Full Text] [Related]
16. Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.
Finklea LB; Mohr MR; Warthan MM; Darrow DH; Williams JV
Pediatr Dermatol; 2010; 27(3):303-5. PubMed ID: 20609155
[TBL] [Abstract][Full Text] [Related]
17. Phakomatosis pigmentovascularis type IIb associated with Klippel-Trénaunay syndrome and congenital triangular alopecia.
Turk BG; Turkmen M; Tuna A; Kilinc Karaarslan I; Ozdemir F
J Am Acad Dermatol; 2011 Aug; 65(2):e46-e49. PubMed ID: 21763548
[No Abstract] [Full Text] [Related]
18. Phakomatosis pigmentovascularis type IIIb: a case associated with Sturge-Weber and Klippel-Trenaunay syndromes.
Diociaiuti A; Guidi B; Aguilar Sanchez JA; Feliciani C; Capizzi R; Amerio P
J Am Acad Dermatol; 2005 Sep; 53(3):536-9. PubMed ID: 16112377
[No Abstract] [Full Text] [Related]
19. Dermal melanocytosis: a clinical spectrum.
Stanford DG; Georgouras KE
Australas J Dermatol; 1996 Feb; 37(1):19-25. PubMed ID: 8936066
[TBL] [Abstract][Full Text] [Related]
20. An infant presenting with skin colour changes.
Smith M; Schofield OM
Clin Exp Dermatol; 2005 May; 30(3):313-5. PubMed ID: 15807708
[No Abstract] [Full Text] [Related]
[Next] [New Search]