Genetic variant analysis of a neonate with Cornelia de Lange syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 449-451, 2020.
Article
en Zh
| WPRIM
| ID: wpr-826558
Biblioteca responsable:
WPRO
ABSTRACT
OBJECTIVE@#To detect pathogenic variant in a neonate suspected for Cornelia de Lange syndrome (CdLS).@*METHODS@#Potential mutations of CdLS-related genes (NIPBL, SMC1A, SMC3, RAD21 and HDAC8) were detected by high-throughput target region capture and next-generation sequencing. Suspected variants was verified by Sanger sequencing.@*RESULTS@#The child was found to harbor a heterozygous splice site variant, c.6109-1G>A, of the NIPBL gene. Sanger sequencing suggested that neither parent has carried the same variant, suggesting that it was de novo. The variant was unreported by HGMD and ExAC database, and was predicted to alter an acceptor splicing site. No pathogenic variants of SMC1A, SMC3, RAD21 and HDAC8 genes were detected.@*CONCLUSION@#The heterozygous c.6109-1G>A splicing variant of the NIPBL gene may underlie the disease in this child. Above finding has expanded the variant spectrum of the NIPBL gene.
Texto completo:
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Índice:
WPRIM
Asunto principal:
Fenotipo
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Variación Genética
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Pruebas Genéticas
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Proteínas de Ciclo Celular
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Síndrome de Cornelia de Lange
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Secuenciación de Nucleótidos de Alto Rendimiento
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Genética
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Mutación
Tipo de estudio:
Prognostic_studies
Límite:
Humans
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Newborn
Idioma:
Zh
Revista:
Chinese Journal of Medical Genetics
Año:
2020
Tipo del documento:
Article