scholarly journals A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioning

2015 ◽  
pp. 1081
Author(s):  
Tadamichi Akagi ◽  
Munemitsu Yoshikawa ◽  
Hideo Nakanishi ◽  
Nagahisa Yoshimura
1996 ◽  
Vol 16 (6) ◽  
pp. 1013-1021 ◽  
Author(s):  
Ilana Ariel ◽  
Dvorah Abeliovich ◽  
Jacob Bar-Ziv ◽  
Abraham Hochberg

Eye ◽  
2021 ◽  
Author(s):  
Inês C. F. Pereira ◽  
Rosanne van de Wijdeven ◽  
Hans M. Wyss ◽  
Henny J. M. Beckers ◽  
Jaap M. J. den Toonder

AbstractGlaucoma is a progressive optic neuropathy that is the second leading cause of preventable blindness worldwide, after cataract formation. A rise in the intraocular pressure (IOP) is considered to be a major risk factor for glaucoma and is associated with an abnormal increase of resistance to aqueous humour outflow from the anterior chamber. Glaucoma drainage devices have been developed to provide an alternative pathway through which aqueous humour can effectively exit the anterior chamber, thereby reducing IOP. These devices include the traditional aqueous shunts with tube-plate design, as well as more recent implants, such as the trabeculectomy-modifying EX-PRESS® implant and the new minimally invasive glaucoma surgery (MIGS) devices. In this review, we will describe each implant in detail, focusing on their efficacy in reducing IOP and safety profile. Additionally, a critical and evidence-based comparison between these implants will be provided. Finally, we will propose potential developments that may help to improve the performance of current devices.


1989 ◽  
Vol 9 (4) ◽  
pp. 1799-1803 ◽  
Author(s):  
A E Reeve ◽  
S A Sih ◽  
A M Raizis ◽  
A P Feinberg

Children with associated Wilms' tumor, aniridia, genitourinary malformations, and mental retardation (WAGR syndrome) frequently have a cytogenetically visible germ line deletion of chromosomal band 11p13. In accordance with the Knudson hypothesis of two-hit carcinogenesis, the absence of this chromosomal band suggests that loss of both alleles of a gene at 11p13 causes Wilms' tumor. Consistent with this model, chromosomes from sporadically occurring Wilms' tumor cells frequently show loss of allelic heterozygosity at polymorphic 11p15 loci, and therefore it has been assumed that allelic loss extends proximally to include 11p13. We report here that in samples from five sporadic Wilms' tumors, allelic loss occurred distal to the WAGR locus on 11p13. In cells from one tumor, mitotic recombination occurred distal to the gamma-globin gene on 11p15.5. Thus, allelic loss in sporadic Wilms' tumor cells may involve a second locus on 11p.


2011 ◽  
Vol 19 (4) ◽  
pp. 492-492 ◽  
Author(s):  
Carol Clericuzio ◽  
Melanie Hingorani ◽  
John A Crolla ◽  
Veronica van Heyningen ◽  
Alain Verloes

2000 ◽  
Vol 9 (4) ◽  
pp. 311-316 ◽  
Author(s):  
Howard R. Desatnik ◽  
Robert E. Foster ◽  
Edward J. Rockwood ◽  
George Baerveldt ◽  
Sanford M. Meyers ◽  
...  
Keyword(s):  

2014 ◽  
pp. 313-318
Author(s):  
Carlo E. Traverso ◽  
Paolo Capris

2018 ◽  
Vol 12 (2) ◽  
pp. 94-98 ◽  
Author(s):  
Kirti Singh ◽  
Ankush Mutreja ◽  
Mainak Bhattacharyya ◽  
Sonal Dangda ◽  
Kirti Jaisingh

2020 ◽  
Vol 27 (2) ◽  
pp. 134-137
Author(s):  
Soojung Lee ◽  
Hyo Jin Kim ◽  
In-sang Jeon

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