The calculation on page 372 referring to the risk of cystic fibrosis in a fetus with echogenic bowel and one detected cystic fibrosis mutation was done incorrectly. This fetus has a prior risk of having cystic fibrosis, given the finding of echogenic bowel, of 0.02 (as was correctly calculated at th
Pitfalls in the interpretation of molecular diagnostic tests
โ Scribed by Bruce R. Korf
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 763 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0887-8013
No coin nor oath required. For personal study only.
โฆ Synopsis
Application of the tools of molecular genetics has vastly increased the power of genetic diagnosis, but also raises significant challenges in interpretation. Molecular tests can be used for diagnosis of an affected individual or determination of carrier status. Either direct mutation analysis or linkage analysis is used in various disorders. Major pitfalls in interpretation of direct tests include mistaking polymorphisms for mutations, in-accurate prognostication based on identification of a mutation, and misinterpretation of the implications of not finding a mutation. Interpretation of linkage tests must take account of the accuracy of proband diagnosis, interpretation of family relationships, and genetic recombination. Cognizance of these issues is vital to avoidance of clinical errors and must be incorporated into genetic counseling. o 1996 Wiley-Liss, Inc.
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