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
- PMID: 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
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 We have obtained data on at least 8 further cases (unpublished).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.
Similar articles
-
Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase.J Med Genet. 1990 Feb;27(2):135-6. doi: 10.1136/jmg.27.2.135. J Med Genet. 1990. PMID: 2319583 Free PMC article.
-
Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q.Am J Med Genet. 1977;1(1):3-19. doi: 10.1002/ajmg.1320010103. Am J Med Genet. 1977. PMID: 610424
-
[Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band].Ann Genet. 1977 Mar;20(1):13-7. Ann Genet. 1977. PMID: 302667 French.
-
Inverted duplication of 8p: ten new patients and review of the literature.Am J Med Genet. 1993 Sep 15;47(4):482-6. doi: 10.1002/ajmg.1320470410. Am J Med Genet. 1993. PMID: 8256810 Review.
-
Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.Am J Med Genet. 1985 Sep;22(1):125-34. doi: 10.1002/ajmg.1320220114. Am J Med Genet. 1985. PMID: 3901750 Review.
Cited by
-
Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase.J Med Genet. 1990 Feb;27(2):135-6. doi: 10.1136/jmg.27.2.135. J Med Genet. 1990. PMID: 2319583 Free PMC article.
-
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.Indian J Pediatr. 1994 May-Jun;61(3):301-6. doi: 10.1007/BF02752230. Indian J Pediatr. 1994. PMID: 7960007 No abstract available.
-
A case of partial trisomy of chromosome 8p associated with autism.J Autism Dev Disord. 2006 Jul;36(5):705-9. doi: 10.1007/s10803-006-0104-3. J Autism Dev Disord. 2006. PMID: 16602035
-
Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.Hum Genet. 1992 May;89(3):307-10. doi: 10.1007/BF00220547. Hum Genet. 1992. PMID: 1601422
-
Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).J Med Genet. 1998 Jul;35(7):604-8. doi: 10.1136/jmg.35.7.604. J Med Genet. 1998. PMID: 9678708 Free PMC article. Review.