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Sturge-Weber syndrome: A review
Pediatric Neurology, 2004Sturge-Weber syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50,000. The disease is characterized by an intracranial vascular anomaly, leptomeningeal angiomatosis, most often involving the occipital and posterior parietal lobes.
Kristin A, Thomas-Sohl +2 more
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Glaucoma in Sturge-Weber Syndrome
Ophthalmology, 1984Trabeculectomy specimens from three eyes with Sturge-Weber syndrome were examined histopathologically. Changes in the trabecular meshwork-Schlemm's canal system were similar to findings in old age and in primary open-angle glaucoma. Two mechanisms for glaucoma are theorized.
G W, Cibis, R C, Tripathi, B J, Tripathi
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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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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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Sturge–Weber syndrome: an update for the pediatrician
World Journal of PediatricsSturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by the simultaneous presence of both cutaneous and extracutaneous capillary malformations. SWS usually presents as a facial port-wine birthmark, with a varying presence of leptomeningeal capillary malformations and ocular vascular abnormalities.
Emilie Dingenen +3 more
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Headache in Sturge‐Weber Syndrome
Headache: The Journal of Head and Face Pain, 1994SYNOPSIS Based on reports of headache in arteriovenous malformations and epilepsy, one would predict that the prevalence of migraine headache in the Sturge‐Weber syndrome would be higher than in the general population. A questionnaire designed to determine the prevalence and type of headache by IHS criteria was sent ...
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Advances in Sturge-Weber syndrome
Current Opinion in Neurology, 2006Recent neuroimaging, clinical and molecular neuropathologic studies have provided new insights into the neurologic aspects of Sturge-Weber syndrome and are summarized here.Molecular studies suggest that abnormal brain blood vessel vasoactive and extracellular matrix molecule expression, as well as aberrant brain vascular innervation, contribute to the ...
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Characteristics, surgical outcomes, and influential factors of epilepsy in Sturge-Weber syndrome
Brain, 2022Meng Zhao, Yongxing Sun, Yuguang Guan
exaly