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|Type:||Artigo de periódico|
|Title:||Prenatal genomic profiling of abdominal wall defects through comparative genomic hybridization: Perspectives for a new diagnostic tool|
|Abstract:||Objectives: To describe the molecular analysis through comparative genomic hybridization (CGH) of fetuses with gastroschisis, and to observe if this technique could improve the resolution of the conventional cytogenetic techniques. Methods: Amniotic analysis of fetuses with gastroschisis, using both conventional (G-banding) and molecular (CGH) cytogenetics assays. Results: All of the seven fetuses studied displayed a normal G-band karyotype. Six fetuses displayed a normal disomic profile through CGH and one sample has displayed ish cgh enh 3q26 -> qter result (ICSN). The fetus with this imbalance of chromosome 3 was re-classified as a ruptured omphalocele, instead of gastroschisis, after birth. Conclusions: The molecular investigation through CGH technique can improve the resolution of the conventional karyotye analysis in cases of abdominal wall defects. Copyright (c) 2007 S. Karger AG, Basel.|
comparative genomic hybridization
|Citation:||Fetal Diagnosis And Therapy. Karger, v. 22, n. 5, n. 361, n. 364, 2007.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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