Literature DB >> 645677

Inherited partial trisomy 8q (22 leads to qter).

P L Townes, M R White.   

Abstract

We report clinical observations and cytogenetic studies of an inherited form of partial trisomy 8q. Although complete trisomy 8 has in recent years proven to be a clinically recognizable syndrome, partial trisomy 8q has been documented in only six individuals. Of these, five were familial and also partially trisomic for chromosome 22. There has been only one prior report of partial trisomy 8q without partial trisomy 22. Review of these cases provides support for the recent suggestion that the phenotype of trisomy 8 may be caused principally by trisomy of the distal segment of 8q.

Mesh:

Year:  1978        PMID: 645677     DOI: 10.1001/archpedi.1978.02120300058012

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  7 in total

1.  Unilateral semicircular canal aplasia in Goldenhar's syndrome.

Authors:  M M Lemmerling; B D Vanzieleghem; G R Mortier; I J Dhooge; M F Kunnen
Journal:  AJNR Am J Neuroradiol       Date:  2000-08       Impact factor: 3.825

2.  A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Authors:  D I Wilson; I E Cross; J A Goodship; J Brown; P J Scambler; H H Bain; J F Taylor; K Walsh; A Bankier; J Burn
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

3.  Spectrum of Di George syndrome in patients with truncus arteriosus: expanded Di George syndrome.

Authors:  D J Radford; L Perkins; R Lachman; Y H Thong
Journal:  Pediatr Cardiol       Date:  1988       Impact factor: 1.655

4.  A child with a recombinant of chromosome 8 inherited from her carrier mother.

Authors:  I C Barnes; D Kumar; R J Bell
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

5.  Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.

Authors:  E S Sachs; G van Waveren
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

6.  Features of DiGeorge syndrome and CHARGE association in five patients.

Authors:  P de Lonlay-Debeney; V Cormier-Daire; J Amiel; V Abadie; S Odent; A Paupe; S Couderc; A L Tellier; D Bonnet; M Prieur; M Vekemans; A Munnich; S Lyonnet
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

7.  Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.

Authors:  F Greenberg; F F Elder; P Haffner; H Northrup; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

  7 in total

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