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Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program.

Four children with biotinidase deficiency were identified during the first year of a neonatal screening program for this disease in the Commonwealth of Virginia. Two unrelated probands were identified among the 81,243 newborn infants who were screened. In addition, two siblings of one of these infants were found to be affected. Both probands had mild neurologic symptoms at two and four months, respectively, and the two older children had more severe neurologic abnormalities, cutaneous findings, and developmental delay at two and three years of age. However, none of the affected children had acute metabolic decompensation. Previous studies have shown that the administration of biotin to affected children can be a lifesaving procedure that can reverse acute symptoms and prevent irreversible neurologic damage. Our findings demonstrate that subtle neurologic abnormalities may appear as early as at two months of age and that developmental abnormalities may occur even in the absence of episodes of overt metabolic decompensation. Since screening and treatment are both inexpensive and effective and the incidence of the disease is well within the range of that of other metabolic diseases for which screening is performed, biotinidase deficiency should be added to the group of metabolic diseases for which screening is done in the neonatal period.

Pubmed ID: 4000223


  • Wolf B
  • Heard GS
  • Jefferson LG
  • Proud VK
  • Nance WE
  • Weissbecker KA


The New England journal of medicine

Publication Data

July 4, 1985

Associated Grants

  • Agency: NCRR NIH HHS, Id: RR 00065

Mesh Terms

  • Amidohydrolases
  • Biotin
  • Biotinidase
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Metabolism, Inborn Errors
  • Neurologic Manifestations
  • Pilot Projects
  • Skin Manifestations
  • Virginia