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Parry-Romberg syndrome associated with unusual intracranial vascular malformations and Phthisis bulbi
Umar Amin Qureshi1, Nisar Ahmad Wani, Uruj Altaf
1S.R. Department of Neonatology and Pediatrics. Sher-i-Kashmir Institute of Medical Sciences (SKIMS), Post Box No 1402. GPO Srinagar, Srinagar, Kashmir, India. dromarqureshi@rediffmail.com
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.
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