Literature DB >> 7702100

Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiency.

M Tuchman1, I Matsuda, A Munnich, S Malcolm, S Strautnieks, T Briede.   

Abstract

We used specific mutation analysis to estimate the proportions of males and females with ornithine transcarbamylase (OTC) deficiency whose mutations occurred in the germ cells of one of the parents. The mutations were identified in the probands, and subsequently carrier testing was performed on their mothers and some of the grandmothers. Of 28 OTC deficient males, only 2 (7%) had sporadic mutations (95% CI, 0.6-18.5%), whereas of 15 OTC deficient females, 12 (80%) had sporadic mutations (95% CI, 63-99%) (P < 0.001). Based on these results we estimated the male/female mutation rate ratio (nu/mu) in the OTC gene to be approximately 52. Assuming a fitness for males with OTC deficiency of 0 and the proportion of new female mutants at 0.80, the estimated fitness of heterozygous females is 0.4. Because of the difference in mutation rates between male and female germ cells, we suggest that 9/10 or higher, rather than the conventional 2/3 proportion, be applied when estimating prior risk of carrier status in a mother of one affected male. The prior risk of a mother of an affected female is much lower, approximately 2/10.

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Year:  1995        PMID: 7702100     DOI: 10.1002/ajmg.1320550118

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  11 in total

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3.  High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders.

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Authors:  P M Green; S Saad; C M Lewis; F Giannelli
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6.  Relative frequency of mutations causing ornithine transcarbamylase deficiency in 78 families.

Authors:  M Tuchman; R J Plante; M A Garcia-Perez; V Rubio
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

7.  Mutations in btk in patients with presumed X-linked agammaglobulinemia.

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8.  Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations.

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9.  Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients.

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10.  Identification of four novel splice site mutations in the ornithine transcarbamylase gene.

Authors:  E Oppliger Leibundgut; B Wermuth; J P Colombo; S Liechti-Gallati
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

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