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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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2015
Sturge-Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis, and impacts approximately 1 in 20000 live births. Sturge-Weber syndrome is not inherited, but rather occurs exclusively sporadically, in both males and females and in all races and ethnic backgrounds. Sturge-Weber syndrome presents at
Mejaški-Bošnjak, Vlatka +5 more
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Sturge-Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis, and impacts approximately 1 in 20000 live births. Sturge-Weber syndrome is not inherited, but rather occurs exclusively sporadically, in both males and females and in all races and ethnic backgrounds. Sturge-Weber syndrome presents at
Mejaški-Bošnjak, Vlatka +5 more
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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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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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Oral Surgery, Oral Medicine, Oral Pathology, 1966
Abstract We have presented a case of Sturge-Weber syndrome which was very bizarre as far as the intraoral hemangioma was concerned. Among the major and minor symptoms of the disease, this patient had convulsions up to the age of 7 years, a very distinct nevus flammeus, electroencephalographic abnormalities, and, of course, the hemangioma.
H E, Royle, R, Lapp, E D, Ferrara
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Abstract We have presented a case of Sturge-Weber syndrome which was very bizarre as far as the intraoral hemangioma was concerned. Among the major and minor symptoms of the disease, this patient had convulsions up to the age of 7 years, a very distinct nevus flammeus, electroencephalographic abnormalities, and, of course, the hemangioma.
H E, Royle, R, Lapp, E D, Ferrara
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Journal of the American Academy of Dermatology, 1999
From the Department of Oral Surgery, Medicine, Pathology, Indiana University,a and the Departments of Dermatologyb and Radiology,c Indiana University Medical Center, Indianapolis; and the University of Missouri School of Medicine, Kansas City.d Reprint requests: Ginat W.
G W, Mirowski +3 more
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From the Department of Oral Surgery, Medicine, Pathology, Indiana University,a and the Departments of Dermatologyb and Radiology,c Indiana University Medical Center, Indianapolis; and the University of Missouri School of Medicine, Kansas City.d Reprint requests: Ginat W.
G W, Mirowski +3 more
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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 ...
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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
SangEun Yeom, Anne M. Comi
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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 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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