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Multidisciplinary, multicenter consensus for the care of patients affected with Sturge-Weber syndrome. [PDF]
Orphanet J Rare DisEl Hachem M +18 more
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Intensity-modulated Radiation Therapy in the Management of Diffuse Choroidal Hemangioma in Sturge-Weber Syndrome. [PDF]
J Ophthalmic Vis ResKarimi S +3 more
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Updates on Sturge-Weber Syndrome
Stroke, 2022Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the brain, skin, and eye. Patients with SWS characteristically have facial capillary malformation, also known as port-wine birthmark, a leptomeningeal vascular malformation seen on contrast-enhanced magnetic resonance imaging
Anne Comi, Sangeun Yeom
exaly +3 more sources
Sturge-Weber syndrome and glaucoma
Optometry - Journal of the American Optometric Association, 2011Sturge-Weber syndrome (SWS) belongs to a group of disorders known as the phakomatoses. It is characterized by congenital hamartomatous malformations involving the eye, skin, and central nervous system. Several ocular complications are associated with SWS, including glaucoma.A 66-year-old black man presented with a history of SWS and previously ...
Joseph Sówka
exaly +3 more sources
Der Radiologe, 2013
Sturge-Weber syndrome (SWS) is a rare congenital disease which affects the brain, the skin and the eyes. It is a sporadically occurring neurocutaneous syndrome affecting the intracerebral veins (venous angiomatosis). The frequency is estimated to be 1 in 50,000 births [1].
W, Reith, U, Yilmaz, A, Zimmer
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Sturge-Weber syndrome (SWS) is a rare congenital disease which affects the brain, the skin and the eyes. It is a sporadically occurring neurocutaneous syndrome affecting the intracerebral veins (venous angiomatosis). The frequency is estimated to be 1 in 50,000 births [1].
W, Reith, U, Yilmaz, A, Zimmer
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The Journal of Dermatologic Surgery and Oncology, 1982
The Sturge‐Weber syndrome is a congenital anomaly that is characterized principally by unilateral angiomatosis of the skin, cerebral meninges and choroid of the eye. It may be attended by mental retardation, convulsions, hemiplegia, and visual disturbances. The complete syndrome is rare. We herewith report a case of the syndrome fairly fully developed.
C E, Kouskoukis, C J, Kanitakis
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The Sturge‐Weber syndrome is a congenital anomaly that is characterized principally by unilateral angiomatosis of the skin, cerebral meninges and choroid of the eye. It may be attended by mental retardation, convulsions, hemiplegia, and visual disturbances. The complete syndrome is rare. We herewith report a case of the syndrome fairly fully developed.
C E, Kouskoukis, C J, Kanitakis
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Archives of Neurology, 1969
THE Sturge-Weber syndrome is usually easy to recognize. It consists of angiomatosis of the upper portion of the face and the cerebral leptomeninges, with progressive calcification in the underlying cerebral cortex. 1 These abnormalities are usually unilatera l .
R H, Wilkins, I A, Brody
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THE Sturge-Weber syndrome is usually easy to recognize. It consists of angiomatosis of the upper portion of the face and the cerebral leptomeninges, with progressive calcification in the underlying cerebral cortex. 1 These abnormalities are usually unilatera l .
R H, Wilkins, I A, Brody
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Child's Nervous System, 2006
Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which are facial, mostly unilateral nevi, leptomeningeal angiomatosis, and congenital glaucoma. The interest of this syndrome for pediatric neurosurgeons is mainly related to the association of SWS with epilepsy in 75-90% of the cases.
C, Di Rocco, G, Tamburrini
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Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which are facial, mostly unilateral nevi, leptomeningeal angiomatosis, and congenital glaucoma. The interest of this syndrome for pediatric neurosurgeons is mainly related to the association of SWS with epilepsy in 75-90% of the cases.
C, Di Rocco, G, Tamburrini
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Archives of Dermatology, 1949
PHAKOMATOSES 1 is the term that has been applied to the neurocutaneous syndromes. This term is derived from the Greek root [unk], which means "mother spot" or "mole" and implies a congenital factor. The three diseases which comprise this group and which have cutaneous lesions are (1) tuberous sclerosis, (2) neurofibromatosis of Von Recklinghausen and ...
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PHAKOMATOSES 1 is the term that has been applied to the neurocutaneous syndromes. This term is derived from the Greek root [unk], which means "mother spot" or "mole" and implies a congenital factor. The three diseases which comprise this group and which have cutaneous lesions are (1) tuberous sclerosis, (2) neurofibromatosis of Von Recklinghausen and ...
openaire +2 more sources
Archives of Neurology And Psychiatry, 1948
IN RECENT years a number of reports have appeared of a condition variously designated as the Sturge-Weber syndrome, Kalischer-Dimitri disease or Brushfield-Wyatt disease. All these terms apparently refer to the same clinical entity. The condition is one of associated facial nevus with homolateral glaucoma and an intracranial pathologic process in the ...
A D, McCOY, H C, VORIS
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IN RECENT years a number of reports have appeared of a condition variously designated as the Sturge-Weber syndrome, Kalischer-Dimitri disease or Brushfield-Wyatt disease. All these terms apparently refer to the same clinical entity. The condition is one of associated facial nevus with homolateral glaucoma and an intracranial pathologic process in the ...
A D, McCOY, H C, VORIS
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