Literature DB >> 3951477

Screening for Duchenne muscular dystrophy: an improved screening test for creatine kinase and its application in an infant screening program.

G Scheuerbrandt, A Lundin, T Lövgren, W Mortier.   

Abstract

A kinetic bioluminescence assay with optimized reagent conditions has been developed for application as a screening test for increased creatine kinase (CK) activities in dried blood spots. This test is used for the early detection of Duchenne muscular dystrophy (DMD) in a voluntary CK screening program in West Germany. Of the 176,600 boys tested up to December 31, 1984, 48 who were less than 6 months old had certain or probable DMD (frequency 1: 3679). In 1983 and 1984, the rate of false positive results was 0.016% for a cut-off activity 300 U/liter and 0.061% for a cut-off activity 180 U/liter. Long-term counseling is offered to families of newly detected DMD patients in order to facilitate the aims of the screening program, namely, avoidance of secondary cases in affected families, early professional care for the sick child, and the early opportunity to make the appropriate decisions for a life with an handicapped child. Two types of a benign hereditary blood anomaly were also detected by CK screening (CK-BB inside erythrocytes or thrombocytes).

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Year:  1986        PMID: 3951477     DOI: 10.1002/mus.880090103

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  14 in total

1.  Screening for Duchenne muscular dystrophy.

Authors:  R A Smith; M Rogers; D M Bradley; J R Sibert; P S Harper
Journal:  Arch Dis Child       Date:  1989-07       Impact factor: 3.791

Review 2.  Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Denise Avard; Bartha M Knoppers
Journal:  Eur J Hum Genet       Date:  2010-03-03       Impact factor: 4.246

3.  Attitudes of mothers to neonatal screening for Duchenne muscular dystrophy.

Authors:  R A Smith; D K Williams; J R Sibert; P S Harper
Journal:  BMJ       Date:  1990-04-28

4.  Early diagnosis and secondary prevention of Duchenne muscular dystrophy.

Authors:  R A Smith; J R Sibert; S J Wallace; P S Harper
Journal:  Arch Dis Child       Date:  1989-06       Impact factor: 3.791

5.  The progress reports on the development of therapies of Duchenne muscular dystrophy.

Authors:  G Scheuerbrandt
Journal:  Acta Myol       Date:  2009-10

6.  Experience with screening newborns for Duchenne muscular dystrophy in Wales.

Authors:  D M Bradley; E P Parsons; A J Clarke
Journal:  BMJ       Date:  1993-02-06

7.  Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK).

Authors:  Stuart J Moat; Donald M Bradley; Rachel Salmon; Angus Clarke; Louise Hartley
Journal:  Eur J Hum Genet       Date:  2013-01-23       Impact factor: 4.246

8.  Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands.

Authors:  A J van Essen; H F Busch; G J te Meerman; L P ten Kate
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

9.  Importance of lower limb surgery in Duchenne muscular dystrophy.

Authors:  R Forst; J Forst
Journal:  Arch Orthop Trauma Surg       Date:  1995       Impact factor: 3.067

10.  Clinic-based infant screening for duchenne muscular dystrophy: a feasibility study.

Authors:  Alissa Cyrus; Natalie Street; Sharon Quary; Julie Kable; Aileen Kenneson; Paul Fernhoff
Journal:  PLoS Curr       Date:  2012-05-02
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