Genetic imprecision: Diagnosis of possible defects often cannot predict prognosis
The author discusses the difficulties in using current genetic information for the detection of hereditary diseases. Although there have been many advances in cytogenetic and molecular testing, the diagnosis of defects does not necessarily predict prognosis. Detection of mutant alleles, mosaicism, familial chromosomal rearrangements and de novo chromosomal rearrangements lends uncertainties to genetic counselling. The problems have been compounded by a lack of follow-up to determine if a defect actually exists in a fetus aborted as a result of counselling; nor has there been long-term follow-up of fetuses carried to term that appear healthy at birth. Disappointments after the discovery of the cystic fibrosis gene were due to discovery of many mutations of the gene, making screening for the disease difficult. Some genetic counselors question the benefits of screening for this disease since with advances in treatment, life span has been lengthened and quality of life has been improved.
- OSTI ID:
- 5622855
- Journal Information:
- Bioscience; (United States), Journal Name: Bioscience; (United States) Vol. 41:5; ISSN BISNA; ISSN 0006-3568
- Country of Publication:
- United States
- Language:
- English
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