Literature DB >> 3621663

Monosomy and trisomy of 15q24----qter in a family with a translocation t(6;15)(p25;q24).

U Kristoffersson, S Heim, N Mandahl, L Sundkvist, J Szelest, I Hägerstrand.   

Abstract

A child with multiple anomalies, including growth retardation, a left-sided diaphragmatic hernia with lung hypoplasia, and cerebral malformations is described. Cytogenetic investigation demonstrated a deletion of the distal part of one chromosome 15, del(15)(q24qter), an aberration not previously described. Family studies revealed that the mother had a balanced translocation, t(6;15)(p25;q24). Two of her subsequent pregnancies resulted in abortions after prenatal diagnosis: one fetus was trisomic for 15q24----qter, while the other had monosomy 15q24----qter and a left-sided diaphragmatic hernia similar to the first child.

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Year:  1987        PMID: 3621663     DOI: 10.1111/j.1399-0004.1987.tb03348.x

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


  10 in total

1.  Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.

Authors:  Molka Kammoun; Wafa Slimani; Hanene Hannachi; Mohamed Bibi; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Pediatr Genet       Date:  2017-04-26

Review 2.  Genetic factors in congenital diaphragmatic hernia.

Authors:  A M Holder; M Klaassens; D Tibboel; A de Klein; B Lee; D A Scott
Journal:  Am J Hum Genet       Date:  2007-04-04       Impact factor: 11.025

3.  An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.

Authors:  E W Roback; A J Barakat; V G Dev; M Mbikay; M Chrétien; M G Butler
Journal:  Am J Med Genet       Date:  1991-01

4.  Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.

Authors:  Shashikant Kulkarni; Prabakaran Nagarajan; Jonathan Wall; Diana J Donovan; Robert L Donell; Azra H Ligon; Sundaresan Venkatachalam; Bradley J Quade
Journal:  Am J Med Genet A       Date:  2008-05-01       Impact factor: 2.802

5.  Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

Authors:  E Blennow; H Telenius; D de Vos; C Larsson; P Henriksson; O Johansson; N P Carter; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

Review 6.  Non-P450 aldehyde oxidizing enzymes: the aldehyde dehydrogenase superfamily.

Authors:  Satori A Marchitti; Chad Brocker; Dimitrios Stagos; Vasilis Vasiliou
Journal:  Expert Opin Drug Metab Toxicol       Date:  2008-06       Impact factor: 4.481

7.  Ring chromosome 15 in a patient with features of Fryns' syndrome.

Authors:  G de Jong; R A Rossouw; A E Retief
Journal:  J Med Genet       Date:  1989-07       Impact factor: 6.318

Review 8.  Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review.

Authors:  Yaobin Liu; Beth Mapow
Journal:  Mol Genet Genomic Med       Date:  2020-05-13       Impact factor: 2.183

9.  A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.

Authors:  Eva Klopocki; Luitgard M Graul-Neumann; Ulrike Grieben; Holger Tönnies; Hans-Hilger Ropers; Denise Horn; Stefan Mundlos; Reinhard Ullmann
Journal:  Eur J Pediatr       Date:  2007-10-12       Impact factor: 3.183

10.  Retinal dehydrogenase-2 is inhibited by compounds that induce congenital diaphragmatic hernias in rodents.

Authors:  Jörg Mey; Randal P Babiuk; Robin Clugston; Wei Zhang; John J Greer
Journal:  Am J Pathol       Date:  2003-02       Impact factor: 4.307

  10 in total

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