Literature DB >> 416414

Newborn screening for maple syrup urine disease (branched-chain ketoaciduria).

E W Naylor, R Guthrie.   

Abstract

Routine newborn screening for maple syrup urine disease (MSUD) has been conducted since 1964, and more than 9 1/2 million newborns throughout the world have been tested with use of a bacterial inhibition assay (BIA) for leucine on dried filter paper blood specimens. Forty-three confirmed cases of the "classical" and the "intermediate" variant forms have been detected. The frequency of MSUD, based on these data, is approximately one in 224,000 newborns. The sensitivity and the specificity of the leucine BIA are demonstrated. There are several problems in routine screening for MSUD, including the fact that the "intermittent" variant form will be missed. A brief summary of the clinical course of the 13 cases detected by our collaborative laboratories is presented.

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Year:  1978        PMID: 416414

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  10 in total

1.  Health factors which may interfere with breast-feeding.

Authors: 
Journal:  Bull World Health Organ       Date:  1989       Impact factor: 9.408

2.  Newborn screening in North America.

Authors:  Bradford L Therrell; John Adams
Journal:  J Inherit Metab Dis       Date:  2007-07-23       Impact factor: 4.982

Review 3.  New developments in neonatal screening.

Authors:  K Bartlett; S J Eaton; M Pourfarzam
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1997-09       Impact factor: 5.747

4.  Outcome of maple syrup urine disease.

Authors:  E R Naughten; J Jenkins; D E Francis; J V Leonard
Journal:  Arch Dis Child       Date:  1982-12       Impact factor: 3.791

Review 5.  The evolution of blood-spot newborn screening.

Authors:  Kaustuv Bhattacharya; Tiffany Wotton; Veronica Wiley
Journal:  Transl Pediatr       Date:  2014-04

6.  Branched-chain Ketoacyl Dehydrogenase Deficiency: Maple Syrup Disease.

Authors:  Kevin A. Strauss; D. Holmes Morton
Journal:  Curr Treat Options Neurol       Date:  2003-07       Impact factor: 3.972

Review 7.  Maple syrup urine disease: mechanisms and management.

Authors:  Patrick R Blackburn; Jennifer M Gass; Filippo Pinto E Vairo; Kristen M Farnham; Herjot K Atwal; Sarah Macklin; Eric W Klee; Paldeep S Atwal
Journal:  Appl Clin Genet       Date:  2017-09-06

8.  Incidence of maple syrup urine disease, propionic acidemia, and methylmalonic aciduria from newborn screening data.

Authors:  Kimberly A Chapman; Gwendolyn Gramer; Sarah Viall; Marshall L Summar
Journal:  Mol Genet Metab Rep       Date:  2018-04-05

9.  Natural history of children and adults with maple syrup urine disease in the NBS-MSUD Connect registry.

Authors:  Aileen Kenneson; Yetsa Osara; Theresa Pringle; Lauren Youngborg; Rani H Singh
Journal:  Mol Genet Metab Rep       Date:  2018-01-28

Review 10.  Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders.

Authors:  Lindsay C Burrage; Sandesh C S Nagamani; Philippe M Campeau; Brendan H Lee
Journal:  Hum Mol Genet       Date:  2014-03-20       Impact factor: 6.150

  10 in total

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