Moyamoya disease causes: Difference between revisions
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== | ==Causes== | ||
The condition is believed to be hereditary and linked to q25.3, on chromosome 17 [http://emedicine.medscape.com/article/1180952-overview#ClinicalCauses]. In Japan the overall incidence is higher (0.35 per 100,000).<ref name="pmid9409395">{{cite journal |author=Wakai K, Tamakoshi A, Ikezaki K, ''et al.'' |title=Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey |journal=[[Clin Neurol Neurosurg]] |volume=99 Suppl 2 |issue= |pages=S1–5 |year=1997 |pmid=9409395 |doi=10.1016/S0303-8467(97)00031-0}}</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 14:56, 26 February 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vishnu Vardhan Serla M.B.B.S. [2]
Causes
The condition is believed to be hereditary and linked to q25.3, on chromosome 17 [3]. In Japan the overall incidence is higher (0.35 per 100,000).[1]
References
- ↑ Wakai K, Tamakoshi A, Ikezaki K; et al. (1997). "Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey". Clin Neurol Neurosurg. 99 Suppl 2: S1–5. doi:10.1016/S0303-8467(97)00031-0. PMID 9409395.