Abstract

Hypospadia is the most common congenital malformation of the urinary tract. It is a malformation with the opening of the urethra proximally from the usual site. The meatal opening can be anywhere alone the shaft of the penis, or in more severe forms, within the scrotum, or in the perineum. Consequently the hypospadias can be distal, medial and proximal. The proximal ones can be penoscrotal (PS), scrotal (SC) and perineal (PE). The cause of hypospadias is largely unknown; however, current epidemiology and laboratory studies have shed new light into the etiology of hypospadias. With recent advancements in molecular biology, microarray technology, it appears that hypospadias is potentially related to disrupted gene expression. Currently, the only available treatment is surgery. The aim of this study was to present our results of the surgical correction of hypospadias and methods used to answer the clinical dilemmas about the gender. Authors have used two methods for a surgical resolution of the hypospadia - one-step operation suggested by Snodgrass and two-step operation, employing free graft suggested by Bracka. Clinical dilemmas regarding the gender were answered using cytogenetic assessment through lymphocyte cultivation method, suggested by Seabright. The cytogenetic assessment was carried in 23 patients with proximal hypospadia (penoscrotal, scrotal and perineal). Characteristic male cariotype (46, XY) was found in 22 patients. In one patient, with scrotal hypospadia, we found the characteristic female cariotype. This patient had testicles. The patient with female cariotype had a TDG gene that determines the differentiation of the testicles. Although surgery remains the only therapy for the treatment of the hypospadias, better understanding of the molecular and hormonal mechanisms behind the diseases may contribute to the prevention and the decrease in the incidence of the malformation. Cytogenetic testing in patients with unclear gender is important in planning further treatment.

Highlights

  • The frequency of hypospadia is : - in boys and the disease is very rare in girls (, )

  • The aim of the study is to asses the suitability of the BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2009; 9 (3): 230-234

  • BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2009; 9 (3): 231-234 group and phytohemagglutinin were added to the Medium

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Summary

Introduction

The frequency of hypospadia is : - in boys and the disease is very rare in girls ( , , ) It is a congenital abnormality in the development of urethra. This abnormality can be manifested in the different development phases, starting from the less severe one, with the opening of the urethra at the level of the head of the penis (glans), through the one with the opening on the body of the penis (penile), to the most severe ones, with the opening of the urethra at the penoscrotal border, scrotum and perineum The aim of the study is to asses the suitability of the BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES 2009; 9 (3): 230-234

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Results

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