Literature DB >> 730164

Partial trisomy 18q in a newborn with typical 18 trisomy phenotype.

J P Fryns, F Detavernier, A van Fleteren, H van den Berghe.   

Abstract

This paper describes a case of partial trisomy of almost the entire long arm of chromosome 18 in a newborn with classic trisomy-18 phenotype, resulting from a de novo unbalanced 181/21p translocation: karyotype: 46,XX,-21,t(18;21)(18qter leads to 18q11 ::21p12 leads to 21qter). A review of the other reported cases of partial trisomy 18 suggests that a critical segment in chromosome 18, corresponding to bands q11-q12, might be responsible for most of the signs of trisomy 18, including failure to thrive and early death.

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Year:  1978        PMID: 730164     DOI: 10.1007/bf00295415

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  9 in total

1.  Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.

Authors:  A M Vianna-Morgante; M J Nozaki; C C Ortega; V Coates; Y Yamamura
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

Review 2.  Congenital malformations in autosomal trisomy syndromes.

Authors:  J Warkany; E Passarge; L B Smith
Journal:  Am J Dis Child       Date:  1966-12

3.  Trisomy 18qter and trisomy mapping of chromosome 18.

Authors:  C Turleau; J de Grouchy
Journal:  Clin Genet       Date:  1977-12       Impact factor: 4.438

4.  Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Authors:  R L Neu; C C Ortega; G A Barg; W Pinto; L I Gardner; W M Howell; T E Denton
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

5.  Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.

Authors:  K Fried; A Bar-Yochai; M Rosenblatt; G Mundel
Journal:  J Med Genet       Date:  1978-02       Impact factor: 6.318

6.  Familial mental retardation in a family with an inherited chromosome rearrangement.

Authors:  A E Chudley; F Bauder; M Ray; P J McAlpine; S D Pena; J L Hamerton
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

7.  Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.

Authors:  L M Stern; A R Mureh
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

8.  A case report of a presumptive +i(18p) associated with serum IgA deficiency.

Authors:  K Ogata; K Iinuma; K Kammura; R Morinaga; J Kato
Journal:  Clin Genet       Date:  1977-03       Impact factor: 4.438

9.  Clinical experience with trisomies 18 and 13.

Authors:  M E Hodes; J Cole; C G Palmer; T Reed
Journal:  J Med Genet       Date:  1978-02       Impact factor: 6.318

  9 in total
  6 in total

Review 1.  Partial trisomy 18q.

Authors:  M Elbistan; S Kucukoduk; N Kara
Journal:  Indian J Pediatr       Date:  1996 May-Jun       Impact factor: 1.967

2.  Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.

Authors:  L Boghosian-Sell; R Mewar; W Harrison; R M Shapiro; E H Zackai; J Carey; L Davis-Keppen; L Hudgins; J Overhauser
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

3.  Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.

Authors:  J P Fryns; A Kleczkowska; E Kubień; H Van den Berghe
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

Review 4.  Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

Authors:  R Mewar; A D Kline; W Harrison; K Rojas; F Greenberg; J Overhauser
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

5.  Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype.

Authors:  J P Fryns; L Vinken; J Marien; H Van den Berghe
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

6.  Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil.

Authors:  Rodrigo Roncato Pereira; Irene Plaza Pinto; Lysa Bernardes Minasi; Aldaires Vieira de Melo; Damiana Mirian da Cruz e Cunha; Alex Silva Cruz; Cristiano Luiz Ribeiro; Cláudio Carlos da Silva; Daniela de Melo e Silva; Aparecido Divino da Cruz
Journal:  PLoS One       Date:  2014-07-25       Impact factor: 3.240

  6 in total

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