Literature DB >> 7740498

Inversion of intron 22 in isolated cases of severe hemophilia A.

E F Tizzano1, M Domènech, M Baiget.   

Abstract

Inversion involving intron 22 is the commonest type of mutation causing severe hemophilia A (HA). We investigated 15 families with isolated cases and 5 families with two or three brothers as the only affected members with hemophilia A, in order to determine the carrier status of the mothers, the origin of the mutation and the presence of germinal mosaicism. Our results show that all mothers tested were carriers of the inversion. In addition, three families whose unique hemophilic member was not available for analysis, were screened for the inversion. In one of these last families, the mother was diagnosed as a carrier and her sister and her niece as non-carriers. DNA haplotype analysis in 8 families with grandparents available for study demonstrated that the inversion originated almost exclusively in male germ cells. These findings have important relevance for genetic counselling in families with an isolated case or to exclude germinal mosaicism. Inversion analysis should constitute the first step in molecular diagnosis of severe hemophilia A.

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Year:  1995        PMID: 7740498

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  6 in total

1.  Prominent Mutation of Intron 22 Inversion in Sporadic Hemophilia: Is It Worth the Antenatal Screening?

Authors:  Werasak Sasanakul; Ampaiwan Chuansumrit; Nongnuch Sirachainan; Praguywan Kadegasem
Journal:  Appl Clin Genet       Date:  2022-05-19

2.  Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.

Authors:  Claudia Pamela Radic; Liliana Carmen Rossetti; Miguel Martín Abelleyro; Miguel Candela; Raúl Pérez Bianco; Miguel de Tezanos Pinto; Irene Beatriz Larripa; Anne Goodeve; Carlos Daniel De Brasi
Journal:  Thromb Haemost       Date:  2012-10-23       Impact factor: 5.249

3.  Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.

Authors:  J Becker; R Schwaab; A Möller-Taube; U Schwaab; W Schmidt; H H Brackmann; T Grimm; K Olek; J Oldenburg
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

4.  Discordant haemophilia A in male siblings due to a de novo mutation on a familial missense mutant allele.

Authors:  A Kentsis; R Anewalt; A Ganguly; J B Allen; E J Neufeld
Journal:  Haemophilia       Date:  2009-04-27       Impact factor: 4.287

5.  Inversions of the factor VIII gene in Japanese patients with severe hemophilia A.

Authors:  Kazuyoshi Fukuda; Hiroyuki Naka; Shogo Morichika; Masaru Shibata; Ichiro Tanaka; Midori Shima; Akira Yoshioka
Journal:  Int J Hematol       Date:  2004-04       Impact factor: 2.490

Review 6.  Eighteen years of molecular genotyping the hemophilia inversion hotspot: from southern blot to inverse shifting-PCR.

Authors:  Liliana C Rossetti; Claudia P Radic; Miguel M Abelleyro; Irene B Larripa; Carlos D De Brasi
Journal:  Int J Mol Sci       Date:  2011-10-24       Impact factor: 5.923

  6 in total

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