Volume 29, Issue 10 (Monthly-Jan 2019)                   Studies in Medical Sciences 2019, 29(10): 716-719 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ghiasian M, Daneshyar S. Gerstmann’s syndrome in non- dominant hemisphere: a case report. Studies in Medical Sciences 2019; 29 (10) :716-719
URL: http://umj.umsu.ac.ir/article-1-4278-en.html
Student Researcher committee, Hamedan University of Medical Sciences ,Hamedan, Iran , s.danshyar72@yahoo.com
Abstract:   (4491 Views)
Gerstmann’s syndrome is caused by a left (dominant) inferior parietal lesion, particularly involving the angular gyrus or subjacent white matter of the left hemisphere. We describe case of an 80 year old right handed man admitted to our hospital with history of sudden onset of blurred vision. At first in neurological examination, he had left hemonymus hemianopia and characteristic features of Gerstmann’s syndrome. In the requested paraclinical test, Computed Tomography (CT) scan showed hypo dense area in the right occipital lobe with expansion to parietal and temporal lobe. Gerstmann’s syndrome is characterized by four symptoms: aghraphia, acalculia, finger agnosia and right-left disorientation. One or more of these manifestations may be associated with word blindness (alexia) and hemonymus hemianopia or lower quadrantanopia.In our case, Gerstmann’s syndrome is caused by a lesion in non -dominant hemisphere, which madethis case worth for reporting.

 
Full-Text [PDF 400 kb]   (1879 Downloads)    
Type of Study: case report | Subject: داخلی مغز و اعصاب

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | Studies in Medical Sciences

Designed & Developed by : Yektaweb