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1.
Ned Tijdschr Geneeskd ; 156(37): A3451, 2012.
Article in Dutch | MEDLINE | ID: mdl-22971426

ABSTRACT

A 21-year-old patient suffering from neurofibromatosis type 1 had received radiotherapy for a chiasm glioma 17 years ago. Fourteen years later, there was progressive deterioration of several neurological functions. MRI scans showed a progressively increasing volume loss of the left hemisphere and stenoses around the circle of Willis with secondary parenchymal effects. Based on conventional cerebral angiography, the diagnosis 'moyamoya syndrome' was made.


Subject(s)
Moyamoya Disease/diagnosis , Neurofibromatosis 1/radiotherapy , Radiation Injuries/diagnosis , Radiotherapy/adverse effects , Female , Humans , Moyamoya Disease/etiology , Radiation Injuries/etiology , Young Adult
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