Literature DB >> 302674

[Chromosome 8 : complete trisomy and segmental trisomies].

M O Rethoré, A Aurias, J Couturier, B Dutrillaux, M Prieur, J Lejeune.   

Abstract

The phenotypic effects of trisomy of various segments of chromosome 8 have been recognized through the analysis of twelve different patients: five mosaic cases of trisomy 8, one case of trisomy for the short arm and the proximal segment of the long arm, two cases of trisomy for a portion of the short arm, and four cases of trisomy for the terminal segment of the long arm. Analysis of the data from the literature and of these personal observations allows the definition of three syndromes: trisomy 8, trisomy 8p and 8q proximal, and trisomy 8q terminal. Three clinical signs are common to the three syndromes: vertebral anomalies, depression of the mesosternum, and bulging of the forehead. This suggests that different segments of chromosome 8 carry genes affecting osseous growth. Trisomy 8p causes, in addition to severe mental deficiency, a thick nose, a large mouth, and microcephaly. Other clinical signs can be assigned to three groups corresponding to the short arm, the proximal part, and the distal part of the long arm.

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Year:  1977        PMID: 302674

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


  18 in total

1.  A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).

Authors:  Molly B Sheridan; Takema Kato; Chad Haldeman-Englert; G Reza Jalali; Jeff M Milunsky; Ying Zou; Ruediger Klaes; Georgio Gimelli; Stefania Gimelli; Robert M Gemmill; Harry A Drabkin; April M Hacker; Julia Brown; David Tomkins; Tamim H Shaikh; Hiroki Kurahashi; Elaine H Zackai; Beverly S Emanuel
Journal:  Am J Hum Genet       Date:  2010-07-30       Impact factor: 11.025

2.  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

3.  Radiological features in trisomy 8.

Authors:  M C Silengo; G F Davi; P Franceschini
Journal:  Pediatr Radiol       Date:  1979-04-19

4.  Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)mat.

Authors:  G I Lazjuk; I W Lurie; Y I Usova; D B Gurevich; M K Nedzved
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

Review 5.  Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism.

Authors:  E M Kuhn; G E Sarto; B J Bates; E Therman
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

6.  Familial partial trisomy 8p without dysmorphic features and only mild mental retardation.

Authors:  J J Engelen; C E de Die-Smulders; J M Sijstermans; L E Meers; J C Albrechts; A J Hamers
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

7.  Trisomy for 8p21 leads to pter owing to a familial translocation.

Authors:  E F Allen; W E Hodgkin
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

8.  Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary tale.

Authors:  J Burn; M Baraitser; D T Hughes; P Saldana-Garcia; J F Taylor
Journal:  Pediatr Cardiol       Date:  1984 Jan-Mar       Impact factor: 1.655

9.  Partial trisomy of the short arm of chromosome 8 resulting from balanced maternal translocation.

Authors:  L A Jones; D R Dengler; K Taysi; G D Shackelford; A F Hartmann
Journal:  J Med Genet       Date:  1980-06       Impact factor: 6.318

10.  Systematic analysis of 95 reciprocal translocations of autosomes.

Authors:  A Aurias; M Prieur; B Dutrillaux; J Lejeune
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132

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