Literature DB >> 457136

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

S Ayme, M G Mattei, J F Mattei, F Giraud.   

Abstract

Three patients have been detected because of abnormal phenotypes. Balanced chromosome rearrangements were found in their karyotypes, and in one of the parents in each case. In these three families the association of an abnormal phenotype and a balanced chromosome rearrangement may either be a chance happening or be induced by a submicroscopic loss of chromosome material, for which different position effects may be responsible, according to the case in question. These observations prompt us to ask what decision should be made relative to termination of pregnancy if such a rearrangement is found in amniotic cells in a family with a previous abnormal child.

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Year:  1979        PMID: 457136     DOI: 10.1007/bf00273267

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


  8 in total

1.  De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.

Authors:  E C Jenkins; F M Curcuru-Giordano; S G Krishna; J Cantarella
Journal:  Ann Genet       Date:  1975-06

2.  A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations.

Authors:  J O van Hemel; J P van Biervliet; P W de Jager-van der Grift
Journal:  Clin Genet       Date:  1975-09       Impact factor: 4.438

3.  A mentally retarded child with a translocation involving chromosomes 12 and 19.

Authors:  T W Histinx; F J Gabreëls; F J Rutten; I I Korten; J M Scheres; E M Joosten
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

4.  [De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl].

Authors:  C Stoll; J M Levy
Journal:  Ann Genet       Date:  1974-09

5.  Correlation between euploid structural chromosome rearrangements and mental subnormality in humans.

Authors:  P A Jacobs
Journal:  Nature       Date:  1974-05-10       Impact factor: 49.962

6.  Presumably balanced translocations involving the same band of chromosome No. 4 found in two mentally retarded, dysmorphic individuals.

Authors:  F Skovby; E Niebuhr
Journal:  Ann Genet       Date:  1974-12

7.  Mental retardation associated with "balanced" chromosome rearrangements.

Authors:  S J Funderburk; M A Spence; R S Sparkes
Journal:  Am J Hum Genet       Date:  1977-03       Impact factor: 11.025

8.  Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases.

Authors:  A T Tharapel; R L Summitt; R S Wilroy; P Martens
Journal:  Clin Genet       Date:  1977-04       Impact factor: 4.438

  8 in total
  13 in total

Review 1.  Balanced translocations in mental retardation.

Authors:  Geert Vandeweyer; R Frank Kooy
Journal:  Hum Genet       Date:  2009-04-05       Impact factor: 4.132

2.  Inversion of chromosome 2 (p11p13): frequency and implications for genetic counselling.

Authors:  I M MacDonald; D M Cox
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Authors:  M G Butler; F J Meaney; C G Palmer
Journal:  Am J Med Genet       Date:  1986-03

4.  Fragile chromosome 16(q22) cause a balanced translocation at the same point.

Authors:  J M García-Sagredo; C San Román; M E Gallego Gómez; G Lledo
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Familial paracentric inversion of chromosome 15 (q15q24).

Authors:  G Del Porto; E D'Alessandro; C De Matteis; R D'Innocenzo; M Baldi; A Pachi; F Cappa
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318

6.  Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation.

Authors:  M G Mattei; J F Mattei; R Bernard; F Giraud
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

Review 7.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  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

9.  Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.

Authors:  J F Mattei; M G Mattei; F Giraud
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

10.  The significance of pericentric inversions of chromosome 2.

Authors:  M Djalali; P Steinbach; J Bullerdiek; M Holmes-Siedle; M R Verschraegen-Spae; A Smith
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

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