Mutation analysis for prenatal diagnosis and heterozygote detection of Gaucher disease type III (Norrbottnian type).

Abstract:

:A single base substitution in exon 10 of the glucocerebrosidase gene was detected in families affected by Gaucher disease (GD) type III. This mutation, which results in the substitution of proline for leucine in position 444 of glucocerebrosidase, has been shown to result in type III GD in a Swedish population. Three fetuses at risk for GD type III were diagnosed as homozygous for the mutation and the pregnancies were terminated. In a fourth pregnancy, one parent was excluded as being a carrier and the risk of having a child affected by GD was ignored. Direct analysis of common mutations causal to GD is now available and improves prenatal diagnosis in families where the molecular defect has been characterized.

journal_name

Prenat Diagn

journal_title

Prenatal diagnosis

authors

Dahl N,Wadelius C,Annerén G,Gustavson KH

doi

10.1002/pd.1970120706

subject

Has Abstract

pub_date

1992-07-01 00:00:00

pages

603-8

issue

7

eissn

0197-3851

issn

1097-0223

journal_volume

12

pub_type

杂志文章
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    abstract::Acquired immunodeficiency syndrome (AIDS) was first described in 1981, and continues to be one of the worst global health pandemics in recorded history. Concerted international efforts have helped to increase awareness of human immunodeficiency (HIV) status, improve access to treatment and continuation of therapy to a...

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  • Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y.

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    doi:10.1002/pd.2137

    authors: Gerdes T,Kirchhoff M,Lind AM,Vestergaard Larsen G,Kjaergaard S

    更新日期:2008-12-01 00:00:00

  • Prenatal diagnosis of a partial 6q trisomy: a case report.

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    doi:10.1002/pd.1526

    authors: Valerio D,Di Domenico A,Felicetti M,La Boccetta A,Ferrara C,Antonio N,Borrelli AL

    更新日期:2006-10-01 00:00:00

  • Normal and abnormal fetal cardiac anatomy.

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    更新日期:2004-12-30 00:00:00

  • Differential patterns of prenatal ipsilateral and contralateral lung growth in cases of isolated left-sided congenital diaphragmatic hernia.

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    authors: Phithakwatchara N,Coleman A,Peiro JL,Lee AE,Keswani SG,Kline-Fath B,Lim FY,Shaaban AF

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  • Prenatal ultrasound diagnosis of frontonasal dysplasia.

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    authors: Martinelli P,Russo R,Agangi A,Paladini D

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  • Exomphalos (omphalocele)

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    doi:10.1002/(sici)1097-0223(199812)18:12<1283::aid-pd4

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    更新日期:1998-12-01 00:00:00

  • Reduction of sera requirements in amniotic fluid cell culture.

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    authors: Chang HC,Jones OW

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  • Overcoming number numbness in prenatal risk communication.

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    authors: Pighin S,Bonnefon JF,Savadori L

    更新日期:2011-08-01 00:00:00

  • Maternal anxiety and ultrasound markers for aneuploidy in a multiethnic population.

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    authors: Lee MJ,Roman AS,Lusskin S,Chen D,Dulay A,Funai EF,Monteagudo A

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  • Heat stable and urea resistant alkaline phosphatase in maternal neutrophils from normal and Down syndrome pregnancies.

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    pub_type: 杂志文章

    doi:

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    更新日期:1999-03-01 00:00:00

  • Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.

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    doi:10.1002/pd.794

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    更新日期:2014-10-01 00:00:00

  • Promises, pitfalls and practicalities of prenatal whole exome sequencing.

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    更新日期:2018-01-01 00:00:00

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  • The association of crown-rump length discrepancy with birthweight discordance in spontaneous versus IVF monochorionic twins: a multicenter study.

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    pub_type: 杂志文章,多中心研究

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  • Feto-amniotic shunting--report of the experience of four European centres.

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  • Prenatal diagnosis of congenital mesoblastic nephroma in mid-second trimester by sonography and magnetic resonance imaging.

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    pub_type:

    doi:

    authors:

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