Literature DB >> 22302461

Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.

Beate Schmidt1, Floris Udink ten Cate, Michael Weiss, Udo Koehler.   

Abstract

We report two unbalanced translocations involving the short arms of chromosomes 7 and 18 due to a balanced translocation 7;18 in the mother. Karyotyping and fluorescence in situ hybridization analysis of the female fetus revealed an unbalanced subtelomeric translocation(karyotype 46,XX,der(18)t(7;18)(p22.3;p11.32)mat resulting in a partial trisomy 7p and a partial monosomy 18p.Array comparative genomic hybridization (CGH) detected a4.44-Mb heterozygous duplication at 7p22.3 to 7p22.1 and a0.178-Mb heterozygous deletion at 18p11.32. Clinical characteristics comprised a mildly stenotic bicuspid aortic valve and a small aortic arch without coarctation. The patient's older brother displayed a reciprocal version of her chromosomal aberration (46,XY,der(7)t(7;18)(p22;p11.32) resulting in a partial monosomy 7p and a partial trisomy 18p. Array CGH revealed a 4.75-Mb heterozygous deletion at 7p22.3p22.1 and a 0.579-Mb duplication at 18p11.32. He presented with tetralogy of Fallot, cleft palate, microcephalus without craniosynostosis, growth retardation, ptosis of the right eyelid, right-sided renal agenesis, unilateral cryptorchism,and mental retardation. In this report, we present the clinical phenotype in patients with aberrations of chromosomes 7p and 18p and reviewed the literature to summarize cardiovascular malformations in these patients.

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Year:  2012        PMID: 22302461     DOI: 10.1007/s00431-012-1682-z

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  55 in total

Review 1.  Heart disease associated with deletion of the short arm of chromosome 18.

Authors:  W Pearl
Journal:  Pediatr Cardiol       Date:  1989       Impact factor: 1.655

2.  [A recent case of partial deletion of short arm of chromosome 18].

Authors:  J C Vaillaud; J Martin; N Ayraud
Journal:  Ann Genet       Date:  1970-06

3.  Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).

Authors:  A Kleczkowska; P Decock; H van den Berghe; J P Fryns
Journal:  Genet Couns       Date:  1994

4.  Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation.

Authors:  Ulrika Wester; Marie-Louise Bondeson; Christina Edeby; Göran Annerén
Journal:  Am J Med Genet A       Date:  2006-06-01       Impact factor: 2.802

5.  Use of array comparative genome hybridization in orofacial clefting.

Authors:  Carlos J Gallego; John Grant; Fady M Mikhail; Christina Barger; Nathaniel H Robin
Journal:  J Craniofac Surg       Date:  2010-09       Impact factor: 1.046

6.  Gonadal dysgenesis in del(18p) syndrome.

Authors:  L Telvi; A Bernheim; A Ion; F Fouquet; Y Le Bouc; J L Chaussain
Journal:  Am J Med Genet       Date:  1995-07-17

7.  Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome.

Authors:  Natalia T Leach; Ilse Chudoba; Tasheena V Stewart; Lewis B Holmes; Stanislawa Weremowicz
Journal:  Am J Med Genet A       Date:  2007-07-01       Impact factor: 2.802

Review 8.  Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.

Authors:  U Moog; J J Engelen; C E de Die-Smulders; J C Albrechts; W H Loneus; A A Haagen; E J Raven; A J Hamers
Journal:  Clin Genet       Date:  1994-12       Impact factor: 4.438

Review 9.  Sibs with tetrasomy 18p born to a mother with trisomy 18p.

Authors:  K Takeda; T Okamura; T Hasegawa
Journal:  J Med Genet       Date:  1989-03       Impact factor: 6.318

Review 10.  Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.

Authors:  K A Chotai; L A Brueton; L van Herwerden; C Garrett; G K Hinkel; A Schinzel; R F Mueller; F Speleman; R M Winter
Journal:  Am J Med Genet       Date:  1994-07-01
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  2 in total

1.  Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.

Authors:  Ibtessam R Hussein; Rima S Bader; Adeel G Chaudhary; Randa Bassiouni; Maha Alquaiti; Fai Ashgan; Hans-Juergen Schulten; Mohammad H Al Qahtani
Journal:  Pediatr Cardiol       Date:  2018-03-14       Impact factor: 1.655

2.  Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams' syndrome patients in Saudi Arabia.

Authors:  A Magbooli; E Huwait; A Chaudhary; R Bader; M Gari; F Ashgan; M Alquaiti; A Abuzenadah; M AlQahtani; I R Hussein
Journal:  Mol Cytogenet       Date:  2016-08-12       Impact factor: 2.009

  2 in total

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