| Literature DB >> 7842430 |
K Houkin1, N Tanaka, A Takahashi, H Kamiyama, H Abe, N Kajii.
Abstract
The authors report four cases of familial occurrence of moyamoya disease. Although the pathogenesis of moyamoya disease is not clear, there is extensive evidence that this disease has a tendency to show multifactorial inheritance. Therefore, a screening test for those at high risk, i.e., who have a moyamoya patient among their blood relatives, is clinically important. Magnetic resonance angiography (MRA) successfully revealed abnormal findings specific to moyamoya disease in members of the four probands families. MRA is a powerful and noninvasive way of detecting individuals at high risk of developing moyamoya disease.Entities:
Mesh:
Year: 1994 PMID: 7842430 DOI: 10.1007/bf00303605
Source DB: PubMed Journal: Childs Nerv Syst ISSN: 0256-7040 Impact factor: 1.475