Literature DB >> 3943862

The significance of pericentric inversions of chromosome 2.

M Djalali, P Steinbach, J Bullerdiek, M Holmes-Siedle, M R Verschraegen-Spae, A Smith.   

Abstract

Thirteen new cases of a pericentric inversion 2 collected from different laboratories are reported. In addition 41 cases of a pericentric inversion 2 were reviewed from the literature. The pooled data were analysed using Weinberg's proband method to evaluate the risk of a carrier for either children with congenital anomalies or reproductive wastage. In the "corrected" sample of 166 lifeborn offspring of carriers of a pericentric inversion 2 there were five who showed phenotypic anomalies and two died a few hours after delivery. The reported anomalies are heterogeneous and probably reflect the basic risk of any couple for abnormal lifeborn offspring. There has been no observation of a lifeborn who inherited an unbalanced recombination of a parental pericentric inversion 2. A carrier of a pericentric inversion 2 obviously has an increased risk for reproductive wastage. This is indicated by (1) an increase of the rate of spontaneous abortions and (2) an increase of the rate of index patients ascertained because of previous miscarriages. The risk of a carrier of a pericentric inversion 2 for a spontaneous abortion or a stillbirth may be about twice the basic risk of the general population.

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Year:  1986        PMID: 3943862     DOI: 10.1007/bf00278814

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  29 in total

1.  [PROBABLE PERICENTRIC INVERSION OF THE NO. 2 CHROMOSOME AND CONGENITAL MALFORMATIONS IN A BOY].

Authors:  J DE GROUCHY; I EMERIT; P CORONE; P VERNANT; M LAMY; P SOULIE
Journal:  Ann Genet       Date:  1963

2.  Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case.

Authors:  I Subrt; J Kozák; O Hníková
Journal:  Hum Hered       Date:  1973-04       Impact factor: 0.444

3.  Inherited pericentric inversion of chromosome number two: a linkage study.

Authors:  L R Weitkamp; M K Janzen; S A Guttormsen; H Gershowitz
Journal:  Ann Hum Genet       Date:  1969-07       Impact factor: 1.670

4.  Pierre Robin syndrome in siblings.

Authors:  R P Singh; N T Jaco; V Vigna
Journal:  Am J Dis Child       Date:  1970-12

5.  Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems.

Authors:  D R Romain; C J Chapman; L Columbano-Green; R H Smythe; O Gebbie
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

6.  Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns.

Authors:  F Hecht; B K Hecht
Journal:  Clin Genet       Date:  1984-09       Impact factor: 4.438

7.  Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11 leads to q13) segment of chromosome 2.

Authors:  C Baccichetti; E Lenzini; A Peserico; R Tenconi
Journal:  Clin Genet       Date:  1980-12       Impact factor: 4.438

8.  Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents.

Authors:  S Ayme; M G Mattei; J F Mattei; F Giraud
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

9.  Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.

Authors:  R S Verma; H Dosik; I B Wexler
Journal:  J Genet Hum       Date:  1977-12

10.  Pericentric inversion in chromosome no. 2 as a de novo mutation.

Authors:  U Hesselbjerg; U Friedrich
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

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  8 in total

1.  A human immunoglobulin kappa orphon without sequence defects may be the product of a pericentric inversion.

Authors:  C Huber; R Thiebe; H Hameister; H Smola; E Lötscher; H G Zachau
Journal:  Nucleic Acids Res       Date:  1990-06-25       Impact factor: 16.971

2.  Abnormal chromosome complement resulting from a familial inversion of chromosome 2.

Authors:  S Richter; B Lockwood; D Lockwood; J Allanson
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

3.  On the significance of pericentric inversions of chromosome 2.

Authors:  J Wahlström; M Kyllerman
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

4.  Familial pericentric inversion of chromosome 12.

Authors:  I Voiculescu; G Barbi; G Wolff; P Steinbach; E Back; W Schempp
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

5.  Evolution versus constitution: differences in chromosomal inversion.

Authors:  S Schmidt; U Claussen; T Liehr; A Weise
Journal:  Hum Genet       Date:  2005-05-11       Impact factor: 4.132

6.  Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis.

Authors:  S Saunier; J Calado; F Benessy; F Silbermann; R Heilig; J Weissenbach; C Antignac
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

7.  The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary.

Authors:  J Wienberg; A Jauch; H J Lüdecke; G Senger; B Horsthemke; U Claussen; T Cremer; N Arnold; C Lengauer
Journal:  Chromosome Res       Date:  1994-09       Impact factor: 5.239

8.  Transposition of human immunoglobulin V kappa genes within the same chromosome and the mechanism of their amplification.

Authors:  F J Zimmer; H Hameister; H Schek; H G Zachau
Journal:  EMBO J       Date:  1990-05       Impact factor: 11.598

  8 in total

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