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1.
Chinese Journal of Medical Genetics ; (6): 1195-1198, 2019.
Artigo em Chinês | WPRIM | ID: wpr-799975

RESUMO

Objective@#To carry out variant analysis for a fetus suspected with harlequin ichthyosis (HI).@*Methods@#Whole exome sequencing (WES) was employed to detect potential variant in the fetus. Suspected variant was validated by Sanger sequencing.@*Results@#A homozygous missense variant c. 6858delT (p.F2286fs) was detected in the fetus, for which both parents were heterozygous carriers. Pathological analysis confirmed the diagnosis of HI.@*Conclusion@#The c. 6858delT variant of the ABCA12 gene probably underlies the disease in the fetus.

2.
Chinese Journal of Medical Genetics ; (6): 1195-1198, 2019.
Artigo em Chinês | WPRIM | ID: wpr-781318

RESUMO

OBJECTIVE@#To carry out variant analysis for a fetus suspected with harlequin ichthyosis (HI).@*METHODS@#Whole exome sequencing (WES) was employed to detect potential variant in the fetus. Suspected variant was validated by Sanger sequencing.@*RESULTS@#A homozygous missense variant c.6858delT (p.F2286fs) was detected in the fetus, for which both parents were heterozygous carriers. Pathological analysis confirmed the diagnosis of HI.@*CONCLUSION@#The c.6858delT variant of the ABCA12 gene probably underlies the disease in the fetus.


Assuntos
Feminino , Humanos , Gravidez , Transportadores de Cassetes de Ligação de ATP , Genética , Feto , Testes Genéticos , Heterozigoto , Ictiose Lamelar , Genética , Diagnóstico Pré-Natal
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