Evidence of glutamatergic dysfunction in orbital frontal cortex and left temporal lobe in schizophrenia

1988 ◽  
Vol 1 (2-3) ◽  
pp. 142-143
2021 ◽  
Author(s):  
Greta Tuckute ◽  
Alexander Paunov ◽  
Hope Kean ◽  
Hannah Small ◽  
Zachary Mineroff ◽  
...  

High-level language processing is supported by a left-lateralized fronto-temporal brain network. How this network emerges ontogenetically remains debated. Given that frontal cortex in general exhibits protracted development, frontal language areas presumably emerge later and/or mature more slowly than temporal language areas. But are temporal areas necessary for the development of the language areas in the frontal lobe, or do frontal language areas instead emerge independently? We shed light on this question through a case study of an individual (EG) born without a left temporal lobe. We use fMRI methods that have been previously extensively validated for their ability to elicit robust language responses at the individual-subject level. As expected in cases of early left hemisphere (LH) damage, we find that EG has a fully functional language network in her right hemisphere (RH) and performs within the normal range on standardized language assessments. However, her RH frontal language areas have no corresponding LH homotopic areas: no reliable response to language is detected on the lateral surface of EG's left frontal lobe. However, another network implicated in high-level cognition - the domain-general multiple demand, MD, network - is robustly present in both right and left frontal lobes, suggesting that EG's left frontal cortex is capable of supporting non-linguistic cognitive functions. The existence of temporal language areas therefore appears to be a prerequisite for the emergence of the language areas in the frontal lobe.


2008 ◽  
Vol 39 (01) ◽  
Author(s):  
AN Datta ◽  
I Jambaqué ◽  
G Dellatolas ◽  
C Bulteau ◽  
M Fohlen ◽  
...  

2021 ◽  
Vol 49 (1) ◽  
pp. 030006052098281
Author(s):  
Liang Zhang ◽  
Hao Yu ◽  
Dan Li ◽  
Hui Qian ◽  
Yuchao Chen

Epilepsy is a chronic neurological disorder that is characterized by episodes of seizure. Sexual dysfunction has been reported in patients with seizure, which mostly manifests as erectile dysfunction and premature ejaculation in men. In this study, we report the case of a 65-year-old Chinese man with frequent spermatorrhea. Electroencephalography suggested local epilepsy in the left temporal lobe. After treatment with anti-epilepsy drugs, the symptoms disappeared and did not recur. To the best of our knowledge, this is the first reported case of epilepsy-induced spermatorrhea. The symptoms of spermatorrhea are probably a rare manifestation of seizure. When repetitive stereotyped symptoms occur, seizure should be considered, and tentative anti-epileptic treatment may be a good option.


2008 ◽  
Vol 46 (2) ◽  
pp. 455-460 ◽  
Author(s):  
W.C.J. Alpherts ◽  
J. Vermeulen ◽  
P.C. van Rijen ◽  
F.H. Lopes da Silva ◽  
C.W.M. van Veelen

2011 ◽  
Vol 21 (1) ◽  
pp. 94-99 ◽  
Author(s):  
Shigeki Sunaga ◽  
Michiharu Morino ◽  
Taro Kusakabe ◽  
Hidenori Sugano ◽  
Hiroyuki Shimizu

2006 ◽  
Vol 59 (2) ◽  
pp. 335-343 ◽  
Author(s):  
Anthony B. Waites ◽  
Regula S. Briellmann ◽  
Michael M. Saling ◽  
David F. Abbott ◽  
Graeme D. Jackson

1992 ◽  
Vol 50 (4) ◽  
pp. 539-542 ◽  
Author(s):  
Nélida S. Garretto ◽  
David Monteverde ◽  
Héctor Giócoli ◽  
Blanca I. Ravera ◽  
Hugo A. Molina ◽  
...  

Schwannomatosis is a rare disorder, still not quite well defined, seldom described in the literature. In this paper we report the case of male. Patient, 52 years old, who in the last 30 years developed five subcutaneous tumors within his limbs peripheral nerves, which histologically proved to be schwannomas. A brain computed tomography showed a partially calcified tumor in the left temporal lobe which most likely was a meningioma. A thorough clinical examination was unable to find signs of type I or type II neurofibromatosis. The present condition, probably a form of phacomatosis, has to be distinguished from neurofibromatosis and is considered as an independent clinical entity whose origin still awaits further detailed investigations.


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