Literature DB >> 6985008

Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1.

P K Jensen, C Junien, S Despoisse, A Bernsen, T Thelle, U Friedrich, A de la Chapelle.   

Abstract

Two patients with an inverted duplication of bands 8p21-p23 are described. The gene for glutathione reductase (GSR; E.C.1.6.4.2) has previously been localized to band 8p21. In one of the patients subband 8p21.1 was included in the duplication; GSR activity in the red blood cells was increased. In the other patient, subband 8p21.1 was not included in the duplication and GSR activity was normal. This allows GSR to be assigned to subband 8p21.1. Including the present 2 patients, at least 13 cases of this abnormality have been published. We have obtained data on at least 8 further cases (unpublished). We conclude that inv dup (8p) is a non-randomly occurring de novo structural aberration in man. The GSR results in our cases prove that breakpoints can be different in different patients. Clinical symptoms and signs include some common features but show marked interpatient variation which should, at least in part, be caused by the differences in break-points. A detailed collaborative study to determine the clinical and epidemiological features of this entity is recommended.

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Year:  1982        PMID: 6985008

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  6 in total

1.  Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.

Authors:  C M Moore; K Barnum; C I Kaye; K S Kagan-Hallett; J C Liang
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  A case of partial trisomy of chromosome 8p associated with autism.

Authors:  Katerina Papanikolaou; Elena Paliokosta; Jolanda Gyftodimou; Gerassimos Kolaitis; Sofia Vgenopoulou; Catherine Sarri; John Tsiantis
Journal:  J Autism Dev Disord       Date:  2006-07

3.  Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase.

Authors:  N C Nevin; P J Morrison; J Jones; M M Reid
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

4.  Partial trisomy of short arm of chromosome 8 (46,XY, inv dup (8) (p21-->pter) in a Bedouin child with multiple congenital anomalies and mental retardation.

Authors:  A A Redha; D S Murthy; H Kandil; T I Farag; R Usha; S A al-Awadi; L A Jeryan; K al-Nagdy; M el-Ghanem
Journal:  Indian J Pediatr       Date:  1994 May-Jun       Impact factor: 1.967

Review 5.  Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).

Authors:  A S Plomp; J J Engelen; J C Albrechts; C E de Die-Smulders; A J Hamers
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

6.  D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).

Authors:  A Minelli; G Floridia; E Rossi; M Clementi; R Tenconi; L Camurri; F Bernardi; H Hoeller; C Previde Re; P Maraschio
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

  6 in total

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