Screening for biotinidase deficiency in newborns: Worldwide experience

B. Wolf*, G. S. Heard

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

Between January 24, 1984, and December 31, 1988, 29 screening programs or biotinidase deficiency in newborns were established in 12 countries, and 4 396 834 newborns were screened. The worldwide incidence is based on screening programs in Australia, Austria, Canada, Italy, Japan, Mexico, New Zealand, Scotland, Spain, Switzerland, The United States, and West Germany. Biotinidase deficiency was detected in 72 newborns; 32 had profound biotinidase deficiency (< 10% of mean normal activity level) and 40 had partial deficiency (10% to 30% of mean normal activity level). The combined incidence of profound and partial deficiency was 1 case per 61 067 live births (1:49 500 to 1:79 544; 95% confidence interval), the estimated frequency of the recessive allele was 0.0040, and the frequency of heterozygosity was estimated to be 1:123. Profound deficiency occurred in 1 per 137 401 live births (1:109 300 to 1:211 200), and partial deficiency in 1 per 109 921 live births (1:86 600 to 1:159 700). Most available parents of children with profound and partial deficiency had biotinidase activity levels intermediate between zero and mean normal activity levels. Six children with profound deficiency wered symptomatic at, or soon after, the time of diagnosis; no infant with partial deficiency has become symptomatic, but little is known about the natural history of infants with partial deficiency. Most children whose biotinidase deficiency was detected by newborn screening were white, one was black, and one Hispanic; biotinidase deficiency has not been detected in Oriental children. Although 8 pilot programs have terminated, 21 will continue either indefinitely or until predetermined targets are reached, and 3 new programs were scheduled to begin in January 1989. Each state, region, and country must decide whether screening for biotinidase deficiency should be added to its existent program based on the various advantages of screening, the incidence, the availability of resources, and priorities.

Original languageEnglish (US)
Pages (from-to)512-517
Number of pages6
JournalPediatrics
Volume85
Issue number4
StatePublished - 1990

Keywords

  • biotinidase deficiency
  • heritable disorder
  • newborn screening
  • vitamin-responsive disorder

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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