Title: Parry–Romberg syndrome associated with unusual intracranial vascular malformations and Phthisis bulbi
Abstract: Neurovascular anomalies of Parry-Romberg syndrome have been reported infrequently. We report a case of Parry-Romberg syndrome with hypoplastic left internal carotid, middle cerebral, anterior cerebral, posterior communicating and posterior cerebral artery. The patient presented with partial seizures, hemiparesis and phthisis bulbi.
Publication Year: 2010
Publication Date: 2010-02-10
Language: en
Type: article
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 18
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