Results 161 to 170 of about 5,302 (181)
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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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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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Anaesthesia for Sturge-Weber syndrome
European Journal of Anaesthesiology, 1999A 6-month-old boy with Sturge-Weber syndrome was scheduled for congenital glaucoma and left buphthalmus surgery. Physical examination revealed haemangioma throughout the right trigeminal nerve, congenital glaucoma, left megalocornea and bilateral buphthalmus.
A, Ceyhan +4 more
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Advances in Neonatal Care, 2014
Sturge-Weber syndrome (SWS) is a rare, congenital neurocutaneous condition (affecting both the skin and the brain) characterized by a facial port-wine stain located specifically on the ophthalmic branch of the trigeminal nerve, cerebral vascular abnormalities, and potential eye involvement.
Sarah J, Garro, Wanda T, Bradshaw
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Sturge-Weber syndrome (SWS) is a rare, congenital neurocutaneous condition (affecting both the skin and the brain) characterized by a facial port-wine stain located specifically on the ophthalmic branch of the trigeminal nerve, cerebral vascular abnormalities, and potential eye involvement.
Sarah J, Garro, Wanda T, Bradshaw
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Pediatric and Developmental Pathology, 2000
I have no intention of going into the difficult question of the pathology of port-wine mark. The point to which I wish to call particular attention is the probable relationship between the mark and the fits …. From the nature of the fits, and from their mode of onset, I think there can be no doubt that they are due to some cause external to the nerve ...
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I have no intention of going into the difficult question of the pathology of port-wine mark. The point to which I wish to call particular attention is the probable relationship between the mark and the fits …. From the nature of the fits, and from their mode of onset, I think there can be no doubt that they are due to some cause external to the nerve ...
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Seminars in Cutaneous Medicine and Surgery, 2004
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma and choroidal hemangioma) and leptomeningeal angioma. Although the precise pathogenesis is unknown, available data regarding genetics, embryogenesis, and pathologic features are briefly reviewed. Clinical features vary from
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Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma and choroidal hemangioma) and leptomeningeal angioma. Although the precise pathogenesis is unknown, available data regarding genetics, embryogenesis, and pathologic features are briefly reviewed. Clinical features vary from
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Glaucomas: Sturge Weber Syndrome
2009Not only is SWS associated with intracranial and facial angiomas (nevus flammeus, see Fig. 46.1), it can also be associated with several anomalous ocular features. Most frequently, hemangiomas of the lid, episclera or conjunctiva (see Fig. 46.2), iris or ciliary body are present.
Annette Giangiacomo, Anne L. Coleman
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Pediatric Dermatology, 1987
Abstract: The Sturge‐Weber syndrome is characterized by angiomas of the leptomeninges overlying the cerebral cortex in association with a facial nevus flammeus. Although frequently included with other neurocutaneous genodermatoses, the syndrome is almost always sporadic in occurrence.
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Abstract: The Sturge‐Weber syndrome is characterized by angiomas of the leptomeninges overlying the cerebral cortex in association with a facial nevus flammeus. Although frequently included with other neurocutaneous genodermatoses, the syndrome is almost always sporadic in occurrence.
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1996
The number of people with this unusual syndrome is unknown, but it is thought to be a rare condition. Both sexes are affected equally.
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The number of people with this unusual syndrome is unknown, but it is thought to be a rare condition. Both sexes are affected equally.
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