Literature DB >> 1547253

Partial trisomy 11q in a female infant with Robin sequence and congenital heart disease.

R Wallerstein1, F Desposito, H Aviv, M Schenk, D F Wallerstein.   

Abstract

We describe the clinical and cytogenetic findings in a female infant with partial trisomy 11q, Robin sequence, cardiac anomalies, and other minor malformations. We compare the phenotypic similarities of our case to a series by Pihko et al. (1981), who reported on 20 cases with partial trisomy 11q with similar associated craniofacial and cardiac defects. We conclude that genetic etiologies for patients diagnosed with the Robin sequence may be more common than previously believed and that initial karyotyping should be performed to aid both diagnosis and clinical management. In addition, the pattern of Robin sequence and cardiac defects may be specifically suggestive of partial trisomy 11q.

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Year:  1992        PMID: 1547253     DOI: 10.1597/1545-1569_1992_029_0077_ptiafi_2.3.co_2

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  2 in total

1.  At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Authors:  D Smeets; C van Ravenswaaij; J de Pater; K Gerssen-Schoorl; J Van Hemel; G Janssen; A Smits
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

2.  Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3).

Authors:  Rongyu Chen; Chuan Li; Bobo Xie; Jin Wang; Xin Fan; Jingsi Luo; Xuyun Hu; Shaoke Chen; Yiping Shen
Journal:  Mol Cytogenet       Date:  2014-12-24       Impact factor: 2.009

  2 in total

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