Reliable techniques for the prenatal diagnosis of many inherited metabolic disorders have recently been developed. There is little doubt that the list of disorders detectable in utero will continue to expand rapidly with our knowledge of the biochemical basis of inherited disease. New prenatal diagnostic methods will be developed and existing procedures will become safer, more accurate and more readily available. These changes will undoubtedly be accompanied by new developments in the prenatal diagnosis of other types of disorders, including chromosomal abnormalities and congenital malformations. Such developments in the prevention of genetic disease will enable us to offer additional options to our patients and families affected with these often devastating disorders.
|Original language||English (US)|
|Number of pages||14|
|Journal||Clinics in Obstetrics and Gynaecology|
|State||Published - Dec 1 1980|
ASJC Scopus subject areas
- Obstetrics and Gynecology