Moya Moya disease presenting as Chorea: A case report

  • Dr S M Saifullah Quraishi Assistant professor, Kurnool medical college Kurnool, India
  • Dr K M Iqbal Hussain Assosiate professor Kurnool medical college kurnool, India
  • Dr G Rajini Post graduate Student, in medicine Kurnool medical college Kurnool, India
  • Dr Sayeeda Afzal Post graduate student in Paediatric GVR children hospital kurnool, India
Keywords: Moya Moya disease, chorea, involuntary movement

Abstract

Moya moya disease is a rare disease characterized by multiple occlusions of the cerebral circulation with an unusual net like system of collaterals. In Japanese moya moya means HAZY. The disease derives its peculiar name from the angiographic appearance of cerebral vessels in the disease that resembles a `PUFF OF SMOKE`. Ischemic insult is more common in children. Chorea is rarely noted with this disease. When a child presents with chorea, clinicians may attribute this symptom to a number of diseases. Any child with involuntary movements, moya moya disease can be a possibility.

Downloads

Download data is not yet available.

References

1. Han DH, Kwon OK, Byun BJ, Choi BY, Choi CW, Choi JU, Choi SG, Doh JO, Han JW, Jung S, Kang SD, Kim DJ, Kim HI, Kim HD, Kim MC, Kim SC, Kim SC, Kim Y, Kwun BD, Lee BG, Lim YJ, Moon JG, Park HS, Shin MS, Song JH, Suk JS, Yim MB, A co-operative study: clinical characteristics of 334 Korean patients with moyamoya disease treated at neurosurgical institutes (1976–1994). The Korean Society for Cerebrovascular Disease. Acta Neurochir (Wien) 2000;142(11):1263–73.

2. Seol HJ, Wang KC, Kim SK, Hwang YS, Kim KJ, Cho BK. Headache in pediatric moyamoya disease: review of 204 consecutive cases. J Neurosurg 2005;103(Suppl 5):439–42. [PubMed]

3. Watanabe K, Negoro T, Maehara M, Takahashi I, Nomura K, Miura K. Moyamoya disease presenting with chorea. Pediatr Neurol. 1990 Jan- Feb;6(1):40-2. [PubMed]

4. Hany SH, Kim YG, Cha SH, Chung SY. J Neurol Neurosurg Psychiatry 2000;69;6 833-834. [PubMed]

5. Lutterman, J., Scott, M., Nass, R., Geva, T. “Moyamoya syndrome associated with congenital heart disease,” Pediatrics, vol. 101, no. 1, January 1998, Pages 57-60. [PubMed]

6. Choi JU, Kim DS, Kim EY, Lee KC: Natural history of moyamoya disease: comparison of activity of daily living in surgery and non surgery groups. Clin Neurol Neurosurg 1997;99(Suppl 2):S11–18. [PubMed]

7. Scott RM, Smith JL, Robertson RL, Madsen JR, Soriano SG, Rockoff MA. Long-term outcome in children with moyamoya syndrome after cranial revascularization by pial synangiosis. J Neurosurg2004;100(2 Suppl Pediatrics):142–9. [PubMed]

8. Kuroda S, Ishikawa T, Houkin K, Nanba R, Hokari M, Iwasaki Y. Incidence and clinical features of disease progression in adult moyamoya disease Stroke 2005;36(10):2148–53. [PubMed]

9. Fukuyama Y, Umezu R. Clinical and cerebral angiographic evolutions of idiopathic progressive occlusive disease of the circle of Willis (‘‘moyamoya’’disease) in children. Brain Dev 1985;7(1):21–37.
CITATION
DOI: 10.17511/ijmrr.2014.i03.15
Published: 2014-06-30
How to Cite
1.
Quraishi SMS, Hussain KMI, G R, Afzal S. Moya Moya disease presenting as Chorea: A case report. Int J Med Res Rev [Internet]. 2014Jun.30 [cited 2024Jul.3];2(3):256- 258. Available from: https://ijmrr.medresearch.in/index.php/ijmrr/article/view/98
Section
Case Report