Hypospadias

2021 ◽  
pp. 1275-1294
Author(s):  
Simon Wharton ◽  
Khurram Khan ◽  
David Coleman

Hypospadias is a congenital developmental penile anomaly characterized by a ventral ectopically sited meatus and a ventrally split foreskin, with or without ventral curvature. It occurs in about 1 in 125 live male births with both genetic and environmental aetiological factors. Hypospadias is corrected to allow micturition while standing, to achieve a natural appearance, and to allow normal sexual function. Operations to achieve this involve a combination of urethroplasty, glansplasty, and skin cover. Hypospadias repair should result in a straight, symmetrical penis with a natural slit-shaped terminal meatus. Normal function and appearance should be maintained with growth. It may be acceptable to complete the reconstruction by discarding the prepuce to give a circumcised appearance. However, in some cultures most boys are not circumcised and a prepuce reconstruction will be more appropriate.

2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 4507-4507
Author(s):  
R. C. Chen ◽  
J. A. Clark ◽  
S. P. Mitchell ◽  
J. A. Talcott

4507 Background: Although patient-reported treatment outcomes have gained wide acceptance, numerical changes in validated instruments are difficult to interpret by patients and physicians. Using functional categories derived from numerical scales, we report 24- and 36-month outcomes after treatments for localized prostate cancer, presented by patients’ baseline (pre-treatment) functional status, to provide more useful prognostic information and to identify further changes in the third year after treatment. Methods: Using validated symptom indices, we prospectively measured sexual, urinary, and bowel functions of 438 men at baseline, and at fixed intervals post treatment. We translated numerical scores into functional categories: good (normal), intermediate, and poor (severe dysfunction). Results: Abnormal baseline function and surgery in men with normal function uniformly produced poor sexual function ( table ), and more external beam radiotherapy (EBRT) and brachytherapy (BT) patients deteriorated between 24 and 36 months. For those with normal urinary continence, NNSRP (non-nerve sparing radical prostatectomy) produced poor outcomes (26%) more frequently than NSRP (9%) at 24 months and 36 months, despite improvement in some NNSRP patients. Severe incontinence was rare after EBRT (1%) and BT (3%), though slightly more frequent in EBRT patients by 36 months. For patients with normal bowel function, EBRT and BT caused worse outcomes than RP; no change occurred after 24 months. Conclusions: Abnormal baseline sexual function and surgery produced uniformly poor sexual function outcomes and poor function increased significantly between 24 and 36 months after radiation therapy. Significant changes in functional category occurred despite unchanged average numerical scores, indicating that stable numerical indices may conceal significant functional changes. [Table: see text] No significant financial relationships to disclose.


2020 ◽  
Vol 17 (9) ◽  
pp. 1665-1675 ◽  
Author(s):  
Lloyd J.W. Tack ◽  
Alexander Springer ◽  
Stefan Riedl ◽  
Ursula Tonnhofer ◽  
Julia Weninger ◽  
...  

2009 ◽  
Vol 181 (4S) ◽  
pp. 113-114
Author(s):  
Akihiro Nakane ◽  
Yutaro Hayashi ◽  
Satoshi Kurokawa ◽  
Hideyuki Kamisawa ◽  
Makoto Imura ◽  
...  

2004 ◽  
Vol 71 ◽  
pp. 193-202 ◽  
Author(s):  
David R Brown

Prion diseases, also referred to as transmissible spongiform encephalopathies, are characterized by the deposition of an abnormal isoform of the prion protein in the brain. However, this aggregated, fibrillar, amyloid protein, termed PrPSc, is an altered conformer of a normal brain glycoprotein, PrPc. Understanding the nature of the normal cellular isoform of the prion protein is considered essential to understanding the conversion process that generates PrPSc. To this end much work has focused on elucidation of the normal function and activity of PrPc. Substantial evidence supports the notion that PrPc is a copper-binding protein. In conversion to the abnormal isoform, this Cu-binding activity is lost. Instead, there are some suggestions that the protein might bind other metals such as Mn or Zn. PrPc functions currently under investigation include the possibility that the protein is involved in signal transduction, cell adhesion, Cu transport and resistance to oxidative stress. Of these possibilities, only a role in Cu transport and its action as an antioxidant take into consideration PrPc's Cu-binding capacity. There are also more published data supporting these two functions. There is strong evidence that during the course of prion disease, there is a loss of function of the prion protein. This manifests as a change in metal balance in the brain and other organs and substantial oxidative damage throughout the brain. Thus prions and metals have become tightly linked in the quest to understand the nature of transmissible spongiform encephalopathies.


2007 ◽  
Vol 177 (4S) ◽  
pp. 120-120
Author(s):  
Pamela I. Ellsworth ◽  
Anthony Caldamone
Keyword(s):  

2006 ◽  
Vol 175 (4S) ◽  
pp. 425-425
Author(s):  
Nasim Zabihi ◽  
Arthur Mourtzinos ◽  
Mary G. Maher ◽  
Shlomo Raz ◽  
Larissa V. Rodriguez

2005 ◽  
Vol 173 (4S) ◽  
pp. 341-341
Author(s):  
Andrea Salonia ◽  
Marina Pontillo ◽  
Fabio Fabbri ◽  
Giuseppe Zanni ◽  
Rita Daverio ◽  
...  

2010 ◽  
Vol 41 (4) ◽  
pp. 2
Author(s):  
DAMIAN McNAMARA
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document