Skip to main content
Log in

The Maya Behind Moyamoya—The Two Extremes of the Disease

  • Clinical Brief
  • Published:
The Indian Journal of Pediatrics Aims and scope Submit manuscript

Abstract

Two children with moyamoya disease at the extremes of the disease- one with minimal clinical involvement and the other one with profound clinical features are reported with an interesting finding of the collaterals being the reason (maya) behind such varied presentations. To the best of authors’ knowledge this is the first Indian report describing the reason behind the varied presentations of moyamoya disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

References

  1. Fukui M, Kono S, Sueishi K, Ikezaki K. Moyamoya disease. Neuropathology. 2000;20:S61–4.

    Article  PubMed  Google Scholar 

  2. Burke GM, Burke AM, Sherma AK, Hurley MC, Batjer HH, Bendok BR. Moyamoya disease: a summary. Neurosurg Focus. 2009;26:E11.

    Article  PubMed  Google Scholar 

  3. Franco CM, Fukujima MM, de Oliveira Rde M, Gabbai AA. Moyamoya disease: report of three cases in Brazilian patients. Arq Neuropsiquiatr. 1999;57:371–6.

    Article  PubMed  CAS  Google Scholar 

  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 (Moyamoya Disease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg. 1997;99:S238–S40.

    Article  PubMed  Google Scholar 

  5. Smith JL. Understanding and treating moyamoya disease in children. Neurosurg Focus. 2009;26:E4.

    PubMed  Google Scholar 

  6. Ohaegbulam C, Magge S, Scott RM. Moyamoya syndrome. In: McLone DG, ed. Pediatric neurosurgery. Surgery of the developing nervous system. 4th ed. Philadelphia: Saunders; 2001. pp. 1077–92.

    Google Scholar 

  7. Yamauchi T, Houkin K, Tada M, Abe H. Familial occurrence of moyamoya disease. Clin Neurol Neurosurg. 1997;99:S162–7.

    Article  PubMed  Google Scholar 

  8. Tripathi P, Tripathi V, Naik RJ, Patel JM. Moya Moya cases treated with encephaloduroarteriosynangiosis. Indian Pediatr. 2007;44:123–7.

    PubMed  Google Scholar 

  9. Maki Y, Enomoto T. Moyamoya disease. Childs Nerv Syst. 1988;4:204–12.

    Article  PubMed  CAS  Google Scholar 

  10. Mugikura S, Higano S, Shirane R, Fujimura M, Shimanuki Y, Takahashi S. Posterior circulation and high prevalence of ischemic stroke among young pediatric patients with Moyamoya disease: evidence of angiography-based differences by age at diagnosis. Am J Neuroradiol. 2011;32:192–8.

    PubMed  CAS  Google Scholar 

Download references

Conflict of Interest

None.

Role of Funding Source

None.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nandini Vijayakanthi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Vijayakanthi, N., Natarajan, T. The Maya Behind Moyamoya—The Two Extremes of the Disease. Indian J Pediatr 80, 601–603 (2013). https://doi.org/10.1007/s12098-012-0813-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12098-012-0813-x

Keywords

Navigation