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Prenatal Diagnosis of Harlequin Ichthyosis:A Case Report
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作者 Xia Qiu-Ling Wang Xing +1 位作者 Huang Shuai Li Jun-Nan 《Maternal-Fetal Medicine》 2020年第4期244-247,共4页
Harlequin ichthyosis is a severe autosomal recessive skin disorder.Most deaths occur within the first few days after birth,and the survivors still have severe chronic skin disease throughout their lives.Almost all cas... Harlequin ichthyosis is a severe autosomal recessive skin disorder.Most deaths occur within the first few days after birth,and the survivors still have severe chronic skin disease throughout their lives.Almost all cases were associated with a pathogenic variant of adenosine triphosphate binding cassette transporter,subfamily A,member 12(ABCA12)gene.We described a case of HI diagnosed by ultrasound examination during the second-trimester and genetic diagnosis reveal two novel heterozygous ABCA12 mutations c.2563-2570delinsGGCAATT,p.(Leu855Glyfs*13),and c.6116delT,p.(Met2039Argfs*8)by the next-generation DNA sequencing,which further enriched our understanding of the pathogenic variation of ABCA12 gene. 展开更多
关键词 Prenatal diagnosis Harlequin ichthyosis ULTRASOUND GENE adenosine triphosphate binding cassette transporter subfamily A member 12(ABCA12)
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