[Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 28(2): 133-6, 2011 Apr.
Article
en Zh
| MEDLINE
| ID: mdl-21462121
ABSTRACT
OBJECTIVE:
To detect the copy number variation (CNV) of a fetus with interrupted aortic arch and ventricular septal defect, in order to explore the underlying genetic causes of the congenital malformation, and investigate the feasibility of array-based comparative genomic hybridization (array-CGH) in molecular cytogenetic diagnosis.METHODS:
The whole genome of the fetus with de novo apparently balanced translocations [46,XX,t(7;9)(q12;q21)] diagnosed by G-banding was scanned and analyzed by array-CGH, and the copy number variation was confirmed by fluorescence in situ hybridization (FISH).RESULTS:
A pathologic submicroscopic CNV [del(22) (q11.2) (17 370 128-19 790 009, -2.42 Mb)] was identified and mapped by array-CGH. FISH test confirmed the microdeletion detected by array-CGH.CONCLUSION:
The cryptic 22q11.2 deletion might be the reason leading to the congenital malformation of the fetus. This study provides evidence that apparently balanced translocations classified by conventional cytogenetic techniques may host additional submicroscopic CNVs which are not located at the breakpoints. Due to the high-resolution, high-throughput and high-accuracy, array-CGH is considered to be a powerful tool for submicroscopic CNVs detection.
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Hibridación Genómica Comparativa
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Variaciones en el Número de Copia de ADN
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Enfermedades Fetales
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Cardiopatías Congénitas
Tipo de estudio:
Diagnostic_studies
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Prognostic_studies
Límite:
Adult
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Female
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Humans
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Pregnancy
Idioma:
Zh
Año:
2011
Tipo del documento:
Article