Literature DB >> 1618492

Familial pericentric inversion (3)(p12q24).

L Lindberg1, K Pelto, G H Borgström.   

Abstract

A large kindred with a familial pericentric inversion of chromosome 3, (p12q24), was found after an investigation initiated by a young female with three spontaneous first-trimester abortions. Altogether 22 (33%) inversion carriers were discovered, 9 females and 13 males. 6 women and 9 men were included in the fertility and segregation analyses because they were all either sexually mature or past maturity. The abortion frequency was below the average European rate in both the inversion carrier group and the cytogenetically normal relative group; 6%:3%, respectively. The mean numbers of pregnancies and live births (1.8-3.1) did not vary significantly in the two comparison groups. The segregation analysis among the inversion carriers showed a good correspondence to the theoretical 1:1 ratio (16:13). Males and females contributed equally. No duplication/deletion syndromes have been found in the kindred; all family members are phenotypically normal. We report a balanced familial pericentric inversion with no adverse effects. This chromosome aberration could be an example of a harmless chromosome polymorphism.

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Year:  1992        PMID: 1618492     DOI: 10.1007/bf00194317

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


  14 in total

1.  [Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3].

Authors:  A Betz; C Turleau; J de Grouchy
Journal:  Ann Genet       Date:  1974-06

Review 2.  Pericentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français.

Authors: 
Journal:  Ann Genet       Date:  1986

3.  An inherited pericentric chromosomal inversion (46, inv3 (p-q+)) associated with skeletal anomalies.

Authors:  M M Cohen; R G Davidson
Journal:  J Pediatr       Date:  1971-09       Impact factor: 4.406

4.  Pericentric inversion inv(3)(p11q21).

Authors:  F S Spedicato; A Dicomite; R Gaudio
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

5.  A paracentric chromosomal inversion associated with repeated early pregnancy wastage.

Authors:  G Stetten; J A Rock
Journal:  Fertil Steril       Date:  1983-07       Impact factor: 7.329

6.  Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

Authors:  P W Allderdice; N Browne; D P Murphy
Journal:  Am J Hum Genet       Date:  1975-11       Impact factor: 11.025

7.  Chromosome abnormalities in 150 couples with multiple spontaneous abortions.

Authors:  P Husslein; J Huber; P Wagenbichler; W Schnedl
Journal:  Fertil Steril       Date:  1982-03       Impact factor: 7.329

8.  A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

Authors:  J L Hamerton; N Canning; M Ray; S Smith
Journal:  Clin Genet       Date:  1975-10       Impact factor: 4.438

9.  Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation.

Authors:  A V Mikelsaar; T Ilus; S Kivi
Journal:  Hum Genet       Date:  1978-02-23       Impact factor: 4.132

10.  Pericentric inversions in man: personal experience and review of the literature.

Authors:  A Kleczkowska; J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

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  5 in total

1.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndrome.

Authors:  S A Goodart; M G Butler; J Overhauser
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

3.  Paternal pericentric inversion of chromosome 4 as a cause of recurrent pregnancy loss.

Authors:  G C Wolf; J Mao; L Izquierdo; G Joffe
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

4.  Assignment of human satellite 1 DNA as revealed by fluorescent in situ hybridization with oligonucleotides.

Authors:  I Tagarro; J Wiegant; A K Raap; J J González-Aguilera; A M Fernández-Peralta
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

5.  Familial pericentric inversion inv(8)(p23q11).

Authors:  H Boyd; J Kaste; E Hovi; U M Ritanen-Mohammed; H Kääriäinen; A de la Chapelle; A E Lehesjoki
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

  5 in total

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