NDLI: An Infantile Case of Sturge-Weber Syndrome in Association with Klippel-Trenaunay-Weber Syndrome and Phakomatosis Pigmentovascularis

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An Infantile Case of Sturge-Weber Syndrome in Association with Klippel-Trenaunay-Weber Syndrome and Phakomatosis Pigmentovascularis

Content Provider	Semantic Scholar
Author	Lee, Chang-Woo Choi, Du-Young Oh, Yeon-Geun Yoon, Hyang-Suk Kim, Jong-Duk
Copyright Year	2005
Abstract	Sturge-Weber syndrome can be associated with facial port-wine stains and intracranial calcification, and concurrent Klippel-Trenaunay-Weber syndrome has been reported. Klippel-Trenaunay-Weber syndrome is a rare congenital mesodermal phakomatosis characterized by cutaneous hemangiomas, venous varicosities and soft tissue or bone hypertrophy of the affected extremities. This report is presented a rare case of the Sturge-Weber syndrome in combination with the Klippel-Trennaunay syndrome and phakomatosis pigmentovascularis in a 4-month-old infant. He showed nevus flameus on the right leg and both part of the face and back, leptomeningeal angiomatosis on right hemisphere, hypertrophy of the right leg, hemiconvulsion on the left and also evidences of congenital glaucoma and nevus of Ota. Very rare case combined with these three kinds of phakomatosis has been reported.
Starting Page	1082
Ending Page	1084
Page Count	3
File Format	PDF HTM / HTML
PubMed reference number	16361829v1
Volume Number	20
Journal	Journal of Korean medical science
Alternate Webpage(s)	https://www.scienceopen.com/document_file/b1693319-6dad-4c23-ae9d-0e89616927fd/PubMedCentral/b1693319-6dad-4c23-ae9d-0e89616927fd.pdf
Alternate Webpage(s)	http://jkms.org/Synapse/Data/PDFData/0063JKMS/jkms-20-1082.pdf
Language	English
Access Restriction	Open
Subject Keyword	Angiomatosis Glaucoma Hemangioma of skin Hydrophthalmos Hyperostosis Hypertrophy Intracranial Hemorrhages Klippel-Trenaunay-Weber Syndrome Limb structure Melanocytic nevus Neurocutaneous Syndromes Nevus sebaceous Port-Wine Stain Sturge-Weber Syndrome Varicosity Weber ochratoxin A soft tissue
Content Type	Text
Resource Type	Article

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