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[Ischemic stroke in a young woman of Turner syndrome with T1-weighted imaging-pulvinar sign].
- Source :
-
Rinsho shinkeigaku = Clinical neurology [Rinsho Shinkeigaku] 2014; Vol. 54 (5), pp. 440-3. - Publication Year :
- 2014
-
Abstract
- A 39-year-old woman developed right hemiparesis in a few days. Magnetic resonance images revealed cerebral infarction in the territory of the left lenticulostriate artery, and MR angiography showed severe stenosis of the middle and anterior cerebral arteries and moderate one of the vertebral arteries. Bilateral and symmetric T1 hyperintensity in the pulvinar (T1-weighted imaging-pulvinar sign; "T1 pulvinar sign") was detected, which is recognized as a key imaging of Fabry disease. The α-galactosidase A gene analysis, however, showed no mutation. Although specific physical symptoms were solely short stature and oligomenorrhea, the diagnosis of Turner syndrome was confirmed by the chromosome analysis which showed mosaicism of 45XO and 46X,r(X) (60%:40%). To our knowledge, this is the first report of Turner syndrome with "T1 pulvinar sign".
- Subjects :
- Adult
Chromosomes, Human, X genetics
Diagnosis, Differential
Fabry Disease
Female
Humans
Mosaicism
Stroke pathology
Turner Syndrome genetics
Turner Syndrome pathology
Diffusion Magnetic Resonance Imaging
Pulvinar pathology
Stroke diagnosis
Stroke etiology
Turner Syndrome complications
Turner Syndrome diagnosis
Subjects
Details
- Language :
- Japanese
- ISSN :
- 1882-0654
- Volume :
- 54
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Rinsho shinkeigaku = Clinical neurology
- Publication Type :
- Academic Journal
- Accession number :
- 24943083
- Full Text :
- https://doi.org/10.5692/clinicalneurol.54.440