Phakomatosis pigmentovascularis type IIb associated with Klippel–Trénaunay syndrome and congenital triangular alopecia
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference6 articles.
1. Phacomatosis pigmentovascularis type IIIb;Seçkin;Int J Dermatol,2007
2. Loss of heterozygosity in human skin;Happle;J Am Acad Dermatol,1999
3. Vascular disorders of infancy and childhood;Paller,2006
4. Phakomatosis pigmentovascularis: clinical findings in 15 patients and review of the literature;Fernández-Guarino;J Am Acad Dermatol,2008
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Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Congenital triangular alopecia associated with phakomatosis pigmentovascularis type ii along with Klippel Trenaunay syndrome;Indian Dermatology Online Journal;2020
2. Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review;American Journal of Medical Genetics Part A;2019-03-28
3. Port-wine stain as a clue for two rare coexisting entities;BMJ Case Reports;2018-07-13
4. 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;The Journal of Dermatology;2016-07-04
5. A case of phakomatosis pigmentovascularis type II: port-wine stain and dermal melanocytosis with cutis marmorata telangiectatica congenita-like lesions;European Journal of Dermatology;2016-05
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