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Case Report
Moyamoya Disease with Intraventricular Hemorrhage in a Child.
Byoung Hai Ahn, Chung Il Noh, Yong Seung Hwang, Young Soo Yoon
Clin Exp Pediatr. 1983;26(12):1247-1253.   Published online December 31, 1983
A 9-year-old female patient with evidence of intraventricular hemorrhage by computed tomography was subsequently proven to have moyamoya disease by cerebral angiography. Subarachnoid hemorrhage is the most common initial manifestation of moyamoya disease in the adult. However, such presentation seldom occurs in childhood moyamoya disease, and intraventricular hemorrhage has been quite rare in children. The rarity of this manifestation of moyamoya disease and its cause...
A Case of Congenital Ateriovenous Malformation.
Sook Kyeung Jung, Dong Hwan Cho, Jeong Bok Lee, Won Jae Park, Kyeung Soo Park
Clin Exp Pediatr. 1983;26(10):1029-1032.   Published online October 31, 1983
We experienced a case of Congenital Cerebral arteriovenous malformation which produced hematomas in a 9 years old girl. We confirmed the AVM and hematomas in the right frontal area, feeding from the right frontopollar artery, a branch of the right anterior carotid artery, and draining to superior sagittal sinus by carotid angiography & brain C-T. She was treated with, total surgical excision of AVM and...
A Case of Moyamoya Disease with Focal Seizure.
Man Gee Hong, Hak Ki Kim, Kyung Tai Whang, Sung Hoon Cho
Clin Exp Pediatr. 1982;25(10):1053-1057.   Published online October 31, 1982
We experienced a case of Moyamoya syndrome in a 4 year-old girl. The patient was well until 3 years of age when she first experienced numbness of the left arm. After 10 days of above episode, she had tonic-clonic movements of left sided extremities which lasted, approximately 2 hours and followed by paresis. During the following week the second attack of focal seizure followed...
A Case of Moyamoya Disease in Child.
Joong Gon Kim, Sang Il Lee, Baek Youn Choo, Kwang Chan Do, Chong Ku Yun
Clin Exp Pediatr. 1981;24(8):786-790.   Published online August 15, 1981
A childhood case of moyamoya disease with subarachnoid hemorrhage is reported. This patient exhibited left hemiparesis, dysarthria, convulsion and mental retardation. He also had characteristic angiographic picture: occlusion of supraclinoid segment of both internal carotid arteries, combined with collateral networks in the base of brain.