Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/80983
Type: Artigo de periódico
Title: Prenatal diagnosis of a partial trisomy 13q (q14 -> qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization
Author: Machado, IN
Heinrich, JK
Campanhol, C
Rodrigues-Peres, RM
Oliveira, FM
Barini, R
Abstract: Partial trisomy 13q is an uncommon chromosomal abnormality with variable phenotypic expression. We report prenatal diagnosis of partial trisomy 13q in a fetus with partial agenesis of the cerebellar vermis, partial agenesis of the corpus callosum, hydrops and polyhydramnios. G-banding karyotyping, spectral karyotyping and array comparative genomic hybridization (aCGH) analysis of fetal blood were performed. Cytogenetic analysis of fetal blood displayed 46,XX,add(4) (q28). The parental karyotypes were normal. A girl was delivered at 34 weeks gestation; she died within 2 h. Autopsy confirmed all the prenatal findings and also showed agenesis of the diaphragm. Spectral karyotyping identified the additional material's origin as chromosome 13. aCGH was carried out and showed amplification of distal regions of the long arm of chromosome 13 from region 13q14 to qter. This is the first report of a fetus with molecular characterization of a partial trisomy 13q (q14 -> qter), present as a de novo unbalanced translocation at chromosome 4q. This case demonstrates the usefulness of molecular characterization of malformed fetuses for prenatal diagnosis and counseling.
Subject: Partial trisomy 13q
Prenatal diagnosis
SKY
Array comparative genomic hybridization
Corpus callosum agenesis
Dandy-Walker malformation
Country: Brasil
Editor: Funpec-editora
Citation: Genetics And Molecular Research. Funpec-editora, v. 9, n. 1, n. 441, n. 448, 2010.
Rights: fechado
Identifier DOI: 10.4238/vol9-1gmr716
Date Issue: 2010
Appears in Collections:Unicamp - Artigos e Outros Documentos

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