Literature DB >> 1424241

Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.

S Stengel-Rutkowski1, K Lohse, C Herzog, C Apacik, J Couturier, A Albert, B Belohradsky.   

Abstract

Partial trisomy 8qter-->q23 or q24.1 has been reported in 15 literature cases. We add two further case reports here. Patient 1 inherited the derivative (2) of a balanced maternal reciprocal translocation t(2;8)(qter;q2300) after 2:2 disjunction and adjacent-1 segregation, and is trisomic for the segment 8qter-->q2300. Patient 2 inherited a recombinant (8) of a balanced maternal inverted insertion inv ins(8)(q1300;q2300q24.2) and is trisomic for the segment 8q24.2-->q2300. The phenotype of both patients is described and compared to the spectrum of symptoms established from the 15 literature cases. This spectrum contains all features observed with a frequency of > = 50%. Patient 1 had 35% of the features of this spectrum; Patient 2 had 47%. The intrauterine survival probability of unbalanced offspring is assumed to be the same in both cases, as nearly the same segments are trisomic. The pedigrees indicate that the inversion carrier may have a reduced production probability of unbalanced gametes and therefore a reduced risk compared to the translocation carrier.

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Year:  1992        PMID: 1424241     DOI: 10.1111/j.1399-0004.1992.tb03234.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

1.  SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variant.

Authors:  Andrew Dauber; Christelle Golzio; Cécile Guenot; Francine M Jodelka; Maria Kibaek; Susanne Kjaergaard; Bruno Leheup; Danielle Martinet; Malgorzata J M Nowaczyk; Jill A Rosenfeld; Susan Zeesman; Janice Zunich; Jacques S Beckmann; Joel N Hirschhorn; Michelle L Hastings; Sebastien Jacquemont; Nicholas Katsanis
Journal:  Am J Hum Genet       Date:  2013-10-17       Impact factor: 11.025

2.  The novel human MOST-1 (C8orf17) gene exhibits tissue specific expression, maps to chromosome 8q24.2, and is overexpressed/amplified in high grade cancers of the breast and prostate.

Authors:  J M M Tan; E P C Tock; V T K Chow
Journal:  Mol Pathol       Date:  2003-04

3.  A rare interstitial duplication of 8q22.1-8q24.3 associated with syndromic bilateral cleft lip/palate.

Authors:  Regina Ferreira Rezek; Ana Angélica Rodrigues Abbas; Juliana Forte Mazzeu; Siliana Maria Duarte Miranda; Cibele Velloso-Rodrigues
Journal:  Case Rep Dent       Date:  2014-11-25

4.  Mild phenotypes associated with an unbalanced X-autosome translocation, 46,X,der(X)t(X;8)(q28;q13).

Authors:  Takafumi Watanabe; Makiho Ishibashi; Ryota Suganuma; Miki Ohara; Shu Soeda; Hiromi Komiya; Keiya Fujimori
Journal:  Clin Case Rep       Date:  2018-06-24
  4 in total

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