Literature DB >> 2267231

Prenatal diagnosis of a partial 8p trisomy.

A Pezzolo1, M P Bicocchi, C Zampatti, C Cuoco, G Gimelli.   

Abstract

The index patient is a female fetus in which prenatal diagnosis of 8p trisomy was established after amniocentesis at 16 weeks of gestation. This fetus was the unbalanced product of a maternal translocation of 5q/8p (karyotype: 46,XX,t(5;8)(q35;p11). Internal malformations include an anomalous lobature of the right lung, a little and high atrio-ventricular communication, and an anomaly in the number and shape of the aortic semilunar valves. The possible relationship between the phenotype and the chromosomal abnormality is briefly discussed.

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Year:  1990        PMID: 2267231     DOI: 10.1002/pd.1970100809

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

1.  Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.

Authors:  C M Moore; K Barnum; C I Kaye; K S Kagan-Hallett; J C Liang
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development.

Authors:  M C Digilio; A Giannotti; G Floridia; F Uccellatore; R Mingarelli; C Danesino; B Dallapiccola; O Zuffardi
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

  2 in total

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