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Multiple intracranial aneurysms associated with branchio-oto-dysplasia
Journal of Korean Medical Science ; : 245-249, 2001.
Article Dans Anglais | WPRIM | ID: wpr-95262
ABSTRACT
Branchio-oto-dysplasia is characterized by abnormalities of embryonic branchial arch system and deafness inherited as autosomal dominant with variable gene expression. We present a rare case of multiple intracranial aneurysms associated with branchio-oto-dysplasia. A 40-yr-old man with severe headache presented as spontaneous subarachnoid hemorrhage on brain computed tomographic scan. The patient also manifested clinical features of branchio-oto-dysplasia and right hemifacial hypoplasia. Carotid angiogram confirmed an aneurysm in the anterior communicating artery. Intraoperative findings demonstrated multiple aneurysms in the anterior communicating artery and in the left posterior communicating artery, which were clipped successfully. Postoperative course was uneventful. This condition has not been reported previously. We also reviewed literatures to discuss whether the intracranial aneurysm was as a coincidental finding or a part of this malformation.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Hémorragie meningée / Os temporal / Os zygomatique / Angiographie cérébrale / Tomodensitométrie / Anévrysme intracrânien / Syndrome branchio-oto-rénal Limites du sujet: Adulte / Humains langue: Anglais Texte intégral: Journal of Korean Medical Science Année: 2001 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Hémorragie meningée / Os temporal / Os zygomatique / Angiographie cérébrale / Tomodensitométrie / Anévrysme intracrânien / Syndrome branchio-oto-rénal Limites du sujet: Adulte / Humains langue: Anglais Texte intégral: Journal of Korean Medical Science Année: 2001 Type: Article