Preimplantation genetic diagnosis of severe inherited skin diseases

被引:28
作者
McGrath, JA
Handyside, AH
机构
[1] United Med & Dent Sch Guys & St Thomas Hosp, St Thomas Hosp, Dept Obstet & Gynaecol, London SE1 7EH, England
[2] St Johns Inst Dermaol, Dept Cell & Mol Pathol, London, England
关键词
genodermatoses; prenatal diagnosis; embryo;
D O I
10.1111/j.1600-0625.1998.tb00305.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Considerable progress has been made recently in elucidating the molecular pathology underlying several forms of inherited skin diseases. One of the most immediate benefits of these discoveries has been the development of DNA-based prenatal diagnosis in pregnancies at risk for recurrence of a particular disorder. In less than 2 decades, prenatal testing has progressed from mid-trimester fetal skin biopsies or protein analysis in a limited number of conditions to first trimester chorionic villus sampling in a much broader range of genodermatoses. Advances in in vitro fertilization protocols and embryo manipulation technology have further led to the feasibility of even earlier prenatal diagnosis through preimplantation genetic diagnosis. This article details some of the recent advances in genetic skin disease research relevant to prenatal diagnosis and explores the possibilities and practicalities of preimplantation genetic diagnosis in the prevention of these conditions.
引用
收藏
页码:65 / 72
页数:8
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