Abstract
The occurrence in a family of an isolated case of an autosomal dominant disorder with reduced penetrance presents a difficult problem in genetic counselling. It is shown that in such a situation the risk of recurrence in subsequent offspring is given by: (formula; see text) where P is the penetrance (0 less than P less than 1) and f' the relative fitness (0 less than f' less than 1) of affected individuals. In all cases the risks of recurrence will exceed 1 in 20 unless penetrance is high (greater than 0.90) and the relative fitness of affected persons is low (less than 0.6).
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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aylsworth A. S., Kirkman H. N. Genetic counseling for autosomal dominant disorders with incomplete penetrance. Birth Defects Orig Artic Ser. 1979;15(5C):25–38. [PubMed] [Google Scholar]
- Friedman J. M. Genetic counseling for autosomal dominant diseases with a negative family history. Clin Genet. 1985 Jan;27(1):68–71. doi: 10.1111/j.1399-0004.1985.tb00186.x. [DOI] [PubMed] [Google Scholar]
- Nevin N. C., Pearce W. G. Diagnostic and genetical aspects of tuberous sclerosis. J Med Genet. 1968 Dec;5(4):273–280. doi: 10.1136/jmg.5.4.273. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pauli R. M., Motulsky A. G. Risk counselling in autosomal dominant disorders with undetermined penetrance. J Med Genet. 1981 Oct;18(5):340–343. doi: 10.1136/jmg.18.5.340. [DOI] [PMC free article] [PubMed] [Google Scholar]