PRENATAL-DIAGNOSIS IN A FAMILY WITH MITOCHONDRIAL ACETOACETYL-COENZYME A THIOLASE DEFICIENCY WITH THE USE OF THE POLYMERASE CHAIN-REACTION FOLLOWED BY THE HETERODUPLEX DETECTION METHOD

被引：2

作者：

FUKAO, T

WAKAZONO, A

SONG, XQ

YAMAGUCHI, S

ZACHARIAS, R

DONLAN, MA

ORII, T

机构：

[1] SHIMANE MED UNIV,DEPT PEDIAT,SHIMANE,JAPAN

[2] INLAND NW GENET CLIN,WASHINGTON,DC

来源：

PRENATAL DIAGNOSIS | 1995年 / 15卷 / 04期

关键词：

3-KETOTHIOLASE DEFICIENCY; MITOCHONDRIAL ACETOACETYL-COA THIOLASE; PRENATAL DIAGNOSIS; POLYMORPHISM; HETERODUPLEX DETECTION;

D O I：

10.1002/pd.1970150411

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Mitochondrial acetoacetyl-coenzyme A (CoA) thiolase deficiency is an organic aciduria which affects isoleucine and ketone body catabolism. GK16 (the index patient) was affected with this disorder and previous studies had revealed that GK16 was a compound heterozygote with IVS8(+1) gt to tt and A301P mutations. In a subsequent pregnancy, prenatal diagnosis was performed and the fetus's amniocytes were analysed by the polymerase chain reaction (PCR) followed by the heteroduplex detection method on a Mutation Detection Enhancement gel. The fetus was identified as a carrier of the IVS8(+1) mutation. We confirmed the diagnosis by immunoblot analysis of extracted amniocytes and gene analysis with blood filter paper after delivery. This is the first report of prenatal diagnosis of this disorder at the gene level.

引用

页码：363 / 367

页数：5

共 16 条

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