We are in the age of genetic discovery. Now the human genome has been compl
etely sequenced1, there will be increasing understanding and ability to man
ipulate biochemical pathways downstream of genes. At the same time, further
development of in vitro fertilization (IVF) and intracytoplasmic sperm inj
ection (ICSI) will enable procreation in situations that were formerly impo
ssible and when there may be an increased possibility of genetic abnormalit
y. Furthermore, preimplantation diagnosis will enable defects to be diagnos
ed and will give the opportunity for the couple to decide whether to contin
ue with treatment towards a pregnancy or not. Thus, there is a need for cli
nicians to have a good knowledge of the genetic and hereditary aspects of m
ale (and indeed female) infertility and for couples to have access to corre
ct information and expert counselling. Also, there are ethical implications
of these scientific and clinical advances for the future child, the indivi
dual, the couple and society. There is increasing public unease about this
new science of reproduction and, in the UK, there is regulation by law; thu
s, there is a need for clinicians and scientists to give accurate informati
on in everyday language to the public.