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Gorlin-Goltz Syndrome and Stroke: a Case report

Hrvoje Budinčević ; Stroke and Intensive Care Unit. Department of neurology, University Hospital „Sveti Duh“
Katarina Starčević
Ivan Bielen
Vida Demarin

Puni tekst: engleski, PDF (149 KB) str. 209-209 preuzimanja: 367* citiraj
APA 6th Edition
Budinčević, H., Starčević, K., Bielen, I. i Demarin, V. (2014). Gorlin-Goltz Syndrome and Stroke: a Case report. Acta Dermatovenerologica Croatica, 22 (3), 209-209. Preuzeto s https://hrcak.srce.hr/126596
MLA 8th Edition
Budinčević, Hrvoje, et al. "Gorlin-Goltz Syndrome and Stroke: a Case report." Acta Dermatovenerologica Croatica, vol. 22, br. 3, 2014, str. 209-209. https://hrcak.srce.hr/126596. Citirano 27.10.2021.
Chicago 17th Edition
Budinčević, Hrvoje, Katarina Starčević, Ivan Bielen i Vida Demarin. "Gorlin-Goltz Syndrome and Stroke: a Case report." Acta Dermatovenerologica Croatica 22, br. 3 (2014): 209-209. https://hrcak.srce.hr/126596
Harvard
Budinčević, H., et al. (2014). 'Gorlin-Goltz Syndrome and Stroke: a Case report', Acta Dermatovenerologica Croatica, 22(3), str. 209-209. Preuzeto s: https://hrcak.srce.hr/126596 (Datum pristupa: 27.10.2021.)
Vancouver
Budinčević H, Starčević K, Bielen I, Demarin V. Gorlin-Goltz Syndrome and Stroke: a Case report. Acta Dermatovenerol Croat. [Internet]. 2014 [pristupljeno 27.10.2021.];22(3):209-209. Dostupno na: https://hrcak.srce.hr/126596
IEEE
H. Budinčević, K. Starčević, I. Bielen i V. Demarin, "Gorlin-Goltz Syndrome and Stroke: a Case report", Acta Dermatovenerologica Croatica, vol.22, br. 3, str. 209-209, 2014. [Online]. Dostupno na: https://hrcak.srce.hr/126596. [Citirano: 27.10.2021.]

Sažetak

We report on the case of a 32-years old male patient who was previously diagnosed with Gorlin-Goltz syndrome. The patient presented with sudden-onset right-sided hemiparesis, supranuclear facioparesis, and motor aphasia. He was treated with thrombolytic therapy, which successfully alleviated the symptoms. Subsequent radiologic work-up revealed anomalies in the vertebral arteries, a bifid rib, an ischemic lesion in the supply area of the left middle cerebral artery, and falx calcifications. Laboratory tests showed a 4G/4G polymorphism of the plasminogen activator inhibitor 1  (PAI-1) gene whose correlation with stroke is discussed in the article.

 

Ključne riječi
Gorlin-Goltz syndrome; stroke; PAI-1 gene polymorphism

Hrčak ID: 126596

URI
https://hrcak.srce.hr/126596

Posjeta: 591 *