Literature DB >> 3746830

Risk estimation in autosomal dominant disorders with reduced penetrance.

A E Emery.   

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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Year:  1986        PMID: 3746830      PMCID: PMC1049696          DOI: 10.1136/jmg.23.4.316

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  Diagnostic and genetical aspects of tuberous sclerosis.

Authors:  N C Nevin; W G Pearce
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

2.  Genetic counseling for autosomal dominant disorders with incomplete penetrance.

Authors:  A S Aylsworth; H N Kirkman
Journal:  Birth Defects Orig Artic Ser       Date:  1979

3.  Genetic counseling for autosomal dominant diseases with a negative family history.

Authors:  J M Friedman
Journal:  Clin Genet       Date:  1985-01       Impact factor: 4.438

4.  Risk counselling in autosomal dominant disorders with undetermined penetrance.

Authors:  R M Pauli; A G Motulsky
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

  4 in total
  4 in total

1.  Mosaicism in ATP1A3-related disorders: not just a theoretical risk.

Authors:  Marie Hully; Juliette Ropars; Laurence Hubert; Nathalie Boddaert; Marlene Rio; Mathieu Bernardelli; Isabelle Desguerre; Valerie Cormier-Daire; Arnold Munnich; Pascale de Lonlay; Louise Reilly; Claude Besmond; Nadia Bahi-Buisson
Journal:  Neurogenetics       Date:  2016-10-10       Impact factor: 2.660

2.  Recurrence risk of a new dominant mutation in children of unaffected parents.

Authors:  E M Wijsman
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

Review 3.  Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.

Authors:  David N Cooper; Michael Krawczak; Constantin Polychronakos; Chris Tyler-Smith; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2013-07-03       Impact factor: 4.132

4.  Familial recurrences of FOXG1-related disorder: Evidence for mosaicism.

Authors:  Kelly Q McMahon; Apostolos Papandreou; Mandy Ma; Brenda J Barry; Ghayda M Mirzaa; William B Dobyns; Richard H Scott; Natalie Trump; Manju A Kurian; Alex R Paciorkowski
Journal:  Am J Med Genet A       Date:  2015-09-14       Impact factor: 2.802

  4 in total

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