Literature DB >> 7957394

Long-term results of selective screening for inborn errors of metabolism.

W Lehnert1.   

Abstract

Since 1973 the University Children's Hospital of Freiburg has provided a service devoted to selective screening for inborn errors of metabolism with particular emphasis on organic acidurias. Patients to be investigated are preselected by local clinical paediatricians. Between 1973 and the end of 1990, 46,700 specimens from approximately 40,000 patients were screened by the methods listed in Table 1. A total of 464 cases were found consisting of 51 different diseases, 242 cases of 23 different organic acidurias and 222 cases of 28 other inborn errors of metabolism. The number of cases diagnosed parallels the number of patients investigated showing that there is still a real demand for metabolic screening. The number of children to be investigated is steadily increasing. Using the presented and already published data an appraisal of the overall incidence of all organic acidurias (1:6700) has been made as well as of the frequencies of the most common types of these disorders.

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Year:  1994        PMID: 7957394     DOI: 10.1007/BF02138770

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  6 in total

1.  Prenatal diagnosis of nonketotic hyperglycinemia: enzymatic analysis of the glycine cleavage system in chorionic villi.

Authors:  K Hayasaka; K Tada; N Fueki; J Aikawa
Journal:  J Pediatr       Date:  1990-03       Impact factor: 4.406

2.  A simple screening test for medium-chain acyl CoA dehydrogenase deficiency.

Authors:  G Rumsby; J W Seakins; J V Leonard
Journal:  Lancet       Date:  1986-08-23       Impact factor: 79.321

3.  Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia.

Authors:  W Lehnert; L Schuchmann; R Urbánek; H Niederhoff; N Böhm
Journal:  Eur J Pediatr       Date:  1978-07-03       Impact factor: 3.183

4.  [Metabolic disorders of branched-chain amino acids: most common forms of organic aciduria in the neonatal period].

Authors:  W Sperl; W Lehnert
Journal:  Klin Padiatr       Date:  1990 Sep-Oct       Impact factor: 1.349

5.  Seven years of experience with selective screening for organic acidurias.

Authors:  W Lehnert; H Niederhoff
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

6.  Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria.

Authors:  J T Coulombe; V E Shih; H L Levy
Journal:  Pediatrics       Date:  1981-01       Impact factor: 7.124

  6 in total
  11 in total

1.  3-Methylglutaconyl-CoA hydratase deficiency: a new patient with speech retardation as the leading sign.

Authors:  R Ensenauer; C B Müller; K O Schwab; K M Gibson; M Brandis; W Lehnert
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

2.  Selective screening for inborn errors of metabolism: the primary care-based model in rural Crete.

Authors:  A Evangeliou; C Lionis; H Michailidou; M Spilioti; A Kanitsakis; P Nikitakis; N Drakonakis; C Giannakopoulou; S Sbyrakis; A C Sewell; H J Boehles; J Smeitink; R A Wevers
Journal:  J Inherit Metab Dis       Date:  2001-12       Impact factor: 4.982

3.  Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry.

Authors:  Toshiyuki Fukao; Shinsuke Maruyama; Toshihiro Ohura; Yuki Hasegawa; Mitsuo Toyoshima; Antti M Haapalainen; Naomi Kuwada; Mari Imamura; Isao Yuasa; Rik K Wierenga; Seiji Yamaguchi; Naomi Kondo
Journal:  JIMD Rep       Date:  2011-09-06

4.  Diagnosis of major organic acidurias in children: two years experience at a tertiary care centre.

Authors:  M P Narayanan; Vaidyanathan Kannan; K P Vinayan; D M Vasudevan
Journal:  Indian J Clin Biochem       Date:  2011-02-01

5.  KBS-DIAMET: database and expert system for diagnosis and treatment of patients with inborn errors of metabolism.

Authors:  U Mischke; G Fraudendienst-Egger; P Matthis; P Gao; F K Trefz
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

6.  Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria.

Authors:  Jacob Hagen; Heleen te Brinke; Ronald J A Wanders; Alida C Knegt; Esmee Oussoren; A Jeannette M Hoogeboom; George J G Ruijter; Daniel Becker; Karl Otfried Schwab; Ingo Franke; Marinus Duran; Hans R Waterham; Jörn Oliver Sass; Sander M Houten
Journal:  J Inherit Metab Dis       Date:  2015-04-10       Impact factor: 4.982

7.  Isobutyryl-CoA dehydrogenase deficiency: isobutyrylglycinuria and ACAD8 gene mutations in two infants.

Authors:  J O Sass; S Sander; J Zschocke
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

8.  Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency: long-term outcome in a case with neonatal onset.

Authors:  W Lehnert; H Niederhoff; T Suormala; E R Baumgartner
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

9.  Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism.

Authors:  Jorn Oliver Sass; Verena Mohr; Heike Olbrich; Udo Engelke; Judit Horvath; Manfred Fliegauf; Niki Tomas Loges; Susanne Schweitzer-Krantz; Ralf Moebus; Polly Weiler; Andreas Kispert; Andrea Superti-Furga; Ron A Wevers; Heymut Omran
Journal:  Am J Hum Genet       Date:  2006-01-18       Impact factor: 11.025

Review 10.  Selective screening for inborn errors of metabolism--past, present and future.

Authors:  G F Hoffmann
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

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