Results 131 to 140 of about 3,465 (171)
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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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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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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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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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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
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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
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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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Hemispherectomy for Sturge-Weber Syndrome
Pediatric Neurosurgery, 1979Patients with Sturge-Weber disease who have the onset of seizures in infancy invariably face a progressively downhill course which leaves them severely hemiplegic, demented and usually institutionalized because of uncontrolled seizures. During the past 12 years, we have carried out 6 hemispherectomies in infants under 1 year of age who presented with ...
H J, Hoffman +3 more
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Sturge-Weber syndrome in pregnancy
American Journal of Obstetrics and Gynecology, 1995Sturge-Weber syndrome is a rare disease involving a port-wine facial nevus and an associated intracranial venous malformation. There are no reports of this disorder in association with pregnancy in the English literature, and the effects of pregnancy on this syndrome remain unknown.
L A, Dolkart, M, Bhat
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Glaucoma in Sturge-Weber syndrome
Journal of American Association for Pediatric Ophthalmology and Strabismus, 1999In glaucoma associated with Sturge-Weber syndrome (SWS), medical treatment often fails to control intraocular pressure, thus requiring surgical intervention that may result in serious complications.Eighteen consecutive patients with SWS were reviewed retrospectively at the King Khaled Eye Specialist Hospital. An intraocular pressure less than 20 mm Hg,
A H, Awad +3 more
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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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