Infertility and the Chromosomal Abnormalities Publisher



H Akhavizadegan HAMED ; Rm Farsani Reza MOHAMMADI ; P Golmohammadi PEDRAM ; S Van Der Walt SONE
Source: Published:2024

Abstract

Diagnosing the genetic causes of infertility and ensuring the birth of a healthy child is the foremost important role of genetics within the treatment of infertility. Utilizing genetic science can prevent the birth of children with congenital anomalies and chromosomal disarranges. Infertility could be a multifactorial disease that cannot be considered a single and particular cause for all included individuals. Genetic causes of infertility are a part of them. One vital point is that on the off chance that there are hereditary problems within the family, these genetic disarranges have a critical part in infertility and more critically within the health of children resulting from infertility treatments. There are two approaches to treating infertility, some of the time only infertility is treated so that pregnancy happens, but another approach is to guarantee the health of the next generation. It also satisfies the wish of the couple to have a healthy child. Typically, where the part of genetics gets to be more prominent. Genetics’ role is vital in evaluating male infertility. In numerous cases, the results of genetic tests provide data that the possibility gives determination or restriction of the cause of infertility. In this way, couples can accomplish a result that is possible for them. It lets them know their perfect pregnancy chances. In this chapter, genetic causes of infertility as well as disorders and diseases that the way in which infertility is caused have been discussed in detail. © 2024 Elsevier B.V., All rights reserved.