Journals / Causapedia / 2020 / Cilt: 9 - Sayı: 2

Unilateral Moyamoya Disease

Unilateral Moyamoya Hastalığı

Journal
Causapedia
Pages
57–62
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper, we present a 5-year-old male patient with unilateral moyamoya disease who was admitted to our hospital with a complaint of headache.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Moyamoya disease is a rare chronic cerebrovascular disease which is characterized with stenosis and occlusions at the distal part of internal carotid artery and at the proximal part of anterior and middle cerebral arteries.
📊
Key Findings & Data:The most frequent symptoms of onset are hemorrhage in adults and ischemia in children.
💡
Conclusion & Impact:In this paper, we present a 5-year-old male patient with unilateral moyamoya disease who was admitted to our hospital with a complaint of headache.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Moyamoya disease is a rare chronic cerebrovascular disease which is characterized with stenosis and occlusions at the distal part of internal carotid artery and at the proximal part of anterior and middle cerebral arteries. The most frequent symptoms of onset are hemorrhage in adults and ischemia in children. In this paper, we present a 5-year-old male patient with unilateral moyamoya disease who was admitted to our hospital with a complaint of headache.

Özet

Moyamoya hastalığı, internal karotid arterin distali ile ön ve orta serebral arterlerin proksimalinde stenoz veya oklüzyonlarla seyreden nadir kronik bir serebrovasküler hastalıktır. Erişkinlerde hemoraji, çocuklarda iskemi sıklıkla başlangıç semptomlarıdır. Bu yazımızda baş ağrısı şikayeti ile hastanemize başvuran 5 yaşında erkek hastada teşhis edilen bir unilateral moyamoya hastalığı vakası sunuyoruz.

🔖

Cite This Article

AKDENİZ, H., GÜNDÜZ, A. M., TOPRAK, N., ARSLAN, H. (2020). Unilateral Moyamoya Disease. Causapedia, Cilt: 9 - Sayı: 2, 57–62. https://ajindex.com/articles/142153

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Yamamoto M, Aoyagi M, Tijima S. Increase in elastin gene expresion and protein synthesis in arterial smooth muscle cell derived from patients with moyamoya disease. Stroke. 1998;28:1733-8
  2. Suzuki J, Kodowa N. Moyamoya disease. Stroke. 1983;14: 104-9
  3. Gosalakkal JA. Moyamoya disease: a review. Neurol India 2002;50:6–10
  4. Fukui M. Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ('Moyamoya' disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (MoyamoyaDisease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg. 1997;99 (Suppl 2):238-40
  5. Chiu D, Shadden P, Batina P. Clinical features of Moyamoya disease in the United States. Stroke. 1998; 29:1347-51
  6. Houkin K, et al. Surgical therapy for adult moyamoya disease. Stroke. 1996;27:1342-6
  7. Kinugasa K, et al. Surgical treatment of moyamoya disease: Operative technique for encephaloduroarterio-myo-synangiosis, it’s follow-up, clinical results and angiograms. Neurosurgery. 1993;32:527-31
  8. Pereira PL, et al. Pediatric moyamoya syndrome. AJR. 1996;167: 526-8
  9. Suzuki Y, et al. Surgical treatment for pediatric moyamoya disease: Use of the superficial temporal artery for both areas supplied by the anterior and middle cerebral arteries. Neurosurgery. 1997;40:324-30.