A case of adult-onset Sturge-Weber syndrome type III without intracranial calcification, presenting with transient homonymous hemianopia
نویسندگان
چکیده
منابع مشابه
Sturge-Weber syndrome with bilateral intracranial calcification.
Four children affected by Sturge-Weber syndrome and demonstrating bilateral intracranial calcification are described, bringing up to 21 the number of similar reported cases. The frequency of bilateral hemisphere involvement in this syndrome is not known, but it might be as high as 15%. If present, neurosurgical intervention is, in our opinion, contraindicated.
متن کاملSturge – Weber syndrome: A case report
Sturge-Weber angiomatosis is a rare, nonhereditary developmental condition characterized by a hamartomatous vascular proliferation involving the tissues of brain and face. A report of a case with facial port wine stains, gingival overgrowth, and dilated ocular vessels is described.
متن کاملManagement of patient with Sturge-Weber syndrome: a case report
INTRODUCTION Sturge-Weber syndrome sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder. CASE PRESENTATION This is case report of a 18-year-old mentally disabled boy, with long-standing seizures, with a port-wine nevi on the left side of the face along the distribution of trigeminal nerve. Interictal encephalogram showed bilateral slow...
متن کاملIsolated frontal lobe calcification in Sturge-Weber syndrome.
The Sturge-Weber syndrome is a phacomatosis characterized by encephalofacial angiomatosis, seizure disorder, and cortical calcification. There are several cases of atypical or incomplete forms of Sturge-Weber syndrome in which the patient presents with a seizure disorder and cortical calcification. The cortical calcifications have been described in the occipital, parietal, and temporal areas [1...
متن کاملAngiodysplastic Sturge Weber syndrome.
Accepted 19 November 2017 DesCripTion A 3-year-old boy presented with global developmental delay, abnormal craniofacial growth and left focal seizures since infancy. He was the first child of a non-consanguineous couple with unremarkable perinatal period. Family history was non-contributory. On examination, he had macrocephaly (head circumference 55 cm, >3 z-score), extensive port-wine stain di...
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ژورنال
عنوان ژورنال: Rinsho Shinkeigaku
سال: 2021
ISSN: 0009-918X,1882-0654
DOI: 10.5692/clinicalneurol.cn-001473