Abstract

To permit normal postnatal germ cell development, the mammalian testis undergoes a complex, multi-staged process of descent to the scrotum. Failure of any part of this process leads to congenital cryptorchidism, wherein the malpositioned testis finds itself at the wrong temperature after birth, which leads to secondary germ cell loss and later infertility and risk of cancer. Recent studies suggest that neonatal gonocytes transform into the putative spermatogenic stem cells between 3 and 9 months, and this initial postnatal step is deranged in cryptorchid testes. In addition, it is thought the abnormality high temperature may also impair apoptosis of remaining gonocytes, allowing some to persist to become the possible source of carcinoma in situ and malignancy after puberty. The biology of postnatal germ cell development is of intense interest, as it is likely to be the key to the optimal timing for orchidopexy.

Highlights

  • The right way to treat undescended testes (UDT) remains to be solved

  • We will propose in this review that knowledge about early postnatal germ cell development is crucial for the optimal management of UDT

  • We examine the evidence for early postnatal germ cell development to determine what controls these steps and to examine the evidence for early orchidopexy to try and prevent abnormal germ cell development

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Summary

Introduction

The right way to treat undescended testes (UDT) remains to be solved. much is known about the development of the testes and sperm cells, there is a missing link in our knowledge. Recent studies have implicated the very first phases (i.e., in the first year) of postnatal germ cell development in the etiology of the subsequent infertility and risk of malignancy.

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Conclusion
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