Long‐term Follow‐up (18–35 years) of Male Patients with History of Bladder Exstrophy (BE) Repair in Childhood: Erectile Function and Fertility Potential Outcome

2012 ◽  
Vol 9 (5) ◽  
pp. 1466-1472 ◽  
Author(s):  
Hosni Khairy Salem ◽  
Mohammed Eisa
Keyword(s):  
Erectile Function ◽  
Bladder Exstrophy ◽  
Potential Outcome ◽  
Long Term Follow Up ◽  
History Of ◽  
Male Patients ◽  
Fertility Potential

scholarly journals Fertility potential in men with a history of congenital undescended testes: a long-term follow-up study

Andrology ◽  
2012 ◽  
Vol 1 (1) ◽  
pp. 100-108 ◽  
Author(s):  
J. van Brakel ◽  
R. Kranse ◽  
S. M. P. F. de Muinck Keizer-Schrama ◽  
A. E. J. Hendriks ◽  
F. H. de Jong ◽  
...  
Keyword(s):  
Undescended Testes ◽  
Follow Up Study ◽  
Long Term Follow Up ◽  
History Of ◽  
Fertility Potential

scholarly journals One - staged reconstruction of bladder exstrophy in male patients: long - term follow-up outcomes

2017 ◽  
Vol 43 (1) ◽  
pp. 155-162 ◽  
Author(s):  
Amilcar Martins Giron ◽  
◽  
Marcos Figueiredo Mello ◽  
Paulo Afonso Carvalho ◽  
Paulo Renato Marcelo Moscardi ◽  
...  
Keyword(s):  
Bladder Exstrophy ◽  
Long Term Follow Up ◽  
Male Patients ◽  
Staged Reconstruction

scholarly journals Simplex Crumbs Homologue 1 Maculopathy Masquerading as Juvenile X-Linked Retinoschisis in Male Patients

2020 ◽  
Vol 4 (5) ◽  
pp. 437-440
Author(s):  
Daniel J. Oh ◽  
Veeral Sheth ◽  
Gerald A. Fishman ◽  
Michael A. Grassi
Keyword(s):  
Natural History ◽  
Carbonic Anhydrase ◽  
Macular Dystrophy ◽  
Long Term Follow Up ◽  
History Of ◽  
Male Patients ◽  
Unrelated Male ◽  
Good Vision

Purpose: We demonstrate that Crumbs homologue 1 ( CRB1) maculopathy should be considered in the differential of petaloid pigmentary changes in the macula of young children with good vision who may be asymptomatic. Methods: We report on 2 unrelated male patients presenting at a young age with decreased vision from a macular dystrophy due to biallelic CRB1 mutations. Results: In addition to a previously described pathogenic variant, Ile167Gly169del, 2 new pathogenic missense variants in CRB1, Thr745Met and Cys948Tyr, are reported here. Conclusions: Although CRB1 mutations have been more commonly described in retinitis pigmentosa and Leber congenital amaurosis, we demonstrate that mutations in CRB1 can cause a maculopathy in which initial features can resemble juvenile X-linked retinoschisis. We show that the accompanying macular edema is responsive to carbonic anhydrase inhibitors. With long-term follow-up for each case, we illustrate the natural history of CRB1 maculopathy based on clinical examination and diagnostic imaging.

The natural history of pituitary apoplexy: long term follow-up study

2019 ◽  
Author(s):  
Ayesha Shaikh ◽  
Natasha Shrikrishnapalasuriyar ◽  
Giselle Sharaf ◽  
David Price ◽  
Maneesh Udiawar ◽  
...  
Keyword(s):  
Natural History ◽  
Pituitary Apoplexy ◽  
Follow Up Study ◽  
Long Term Follow Up ◽  
History Of

ID: 3524040 THE NATURAL HISTORY OF AMPULLARY ADENOMAS IN FAMILIAL ADENOMATOUS POLYPOSIS SYNDROME: LONG-TERM FOLLOW-UP

2021 ◽  
Vol 93 (6) ◽  
pp. AB350
Author(s):  
Achintya D. Singh ◽  
Amit Bhatt ◽  
Abel Joseph ◽  
Neal Mehta ◽  
Gautam N. Mankaney ◽  
...  
Keyword(s):  
Familial Adenomatous Polyposis ◽  
Natural History ◽  
Adenomatous Polyposis ◽  
Polyposis Syndrome ◽  
Long Term Follow Up ◽  
History Of
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