In vivo analysis and comparison of anterior segment structures of both eyes in unilateral Fuchs’ uveitis syndrome

2019 ◽  
Vol 257 (7) ◽  
pp. 1489-1498 ◽  
Author(s):  
Muhammet Derda Ozer ◽  
Fatih Kebapci ◽  
Muhammed Batur ◽  
Erbil Seven ◽  
Serek Tekin
2019 ◽  
Vol 6 (1) ◽  
pp. 3-9
Author(s):  
Virginia Mares ◽  
Marcio B. Nehemy ◽  
Diva R. Salomão ◽  
Shannon Goddard ◽  
Jaime Tesmer ◽  
...  

Objective: To demonstrate the multimodal imaging and histopathology of Berger’s space. Methods: We conducted a retrospective in vivo analysis of 4 patients demonstrating Berger’s space with intraocular pathological conditions, documented by slit-lamp biomicroscopic photography and, in 2 patients, also by optical coherence tomography (OCT). Additionally, we carried out a retrospective histological study of 7 enucleated eyes with retinoblastoma demonstrating Berger’s space. A review of the literature was also performed. Results: Two eyes had slit-lamp photographs. One case showed Berger’s space surrounded by vitreous hemorrhage. In the other case, amyloid was trapped within Berger’s space. In another 2 eyes that were pseudophakic, Berger’s space was visible on anterior segment OCT. One had amyloid trapped in Berger’s space that could be seen with OCT. The histological review of the 7 enucleated eyes with advanced retinoblastoma demonstrated the presence of pyknotic cells in Berger’s space. Conclusions: Berger’s space is an actual space in pathological conditions and can be an important site of pathology. Additionally, to our knowledge, this is the first time that Berger’s space has been documented by anterior segment OCT in a clinical setting.


2020 ◽  
Vol 64 (2) ◽  
pp. 251-261
Author(s):  
Jessica E. Fellmeth ◽  
Kim S. McKim

Abstract While many of the proteins involved in the mitotic centromere and kinetochore are conserved in meiosis, they often gain a novel function due to the unique needs of homolog segregation during meiosis I (MI). CENP-C is a critical component of the centromere for kinetochore assembly in mitosis. Recent work, however, has highlighted the unique features of meiotic CENP-C. Centromere establishment and stability require CENP-C loading at the centromere for CENP-A function. Pre-meiotic loading of proteins necessary for homolog recombination as well as cohesion also rely on CENP-C, as do the main scaffolding components of the kinetochore. Much of this work relies on new technologies that enable in vivo analysis of meiosis like never before. Here, we strive to highlight the unique role of this highly conserved centromere protein that loads on to centromeres prior to M-phase onset, but continues to perform critical functions through chromosome segregation. CENP-C is not merely a structural link between the centromere and the kinetochore, but also a functional one joining the processes of early prophase homolog synapsis to late metaphase kinetochore assembly and signaling.


2005 ◽  
Vol 173 (4S) ◽  
pp. 287-287
Author(s):  
Anhur L. Burnett ◽  
Hunter C. Champion ◽  
Robyn E. Becker ◽  
Melissa F. Kramer ◽  
Tongyun Liu ◽  
...  

Pneumologie ◽  
2017 ◽  
Vol 71 (S 01) ◽  
pp. S1-S125
Author(s):  
S Berger ◽  
C Gökeri ◽  
U Behrendt ◽  
SM Wienhold ◽  
J Lienau ◽  
...  

Diabetes ◽  
1993 ◽  
Vol 42 (7) ◽  
pp. 956-965 ◽  
Author(s):  
B. A. Zinker ◽  
D. B. Lacy ◽  
D. Bracy ◽  
J. Jacobs ◽  
D. H. Wasserman

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