Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Families who have had a child die of a severe, maternally inherited mitochondrial DNA (mtDNA) disease are usually desperate to avoid having further affected children. Here we discuss the problems of applying classical genetic management to mtDNA diseases (Poulton and Turnbull, 2000) and the biology underlying these problems. We explain why these disorders have lagged so far behind the genetics revolution. We then outline the directions in which management is likely to develop, including the use of preimplantation genetic diagnosis (PGD).

More information Original publication

DOI

10.1016/S0070-2153(06)77008-9

Type

Journal article

Publication Date

2007-01-01T00:00:00+00:00

Volume

77

Pages

213 - 225

Total pages

12

Keywords

Animals, Blastocyst, Chorionic Villi Sampling, DNA, Mitochondrial, Disease Susceptibility, Humans, Mitochondrial Diseases