Newborn screening for cystic fibrosis in Alberta: Two years of experience.

نویسندگان

  • Margaret Lilley
  • Susan Christian
  • Stacey Hume
  • Patrick Scott
  • Mark Montgomery
  • Lisa Semple
  • Peter Zuberbuhler
  • Joan Tabak
  • Fiona Bamforth
  • Martin J Somerville
چکیده

On April 1, 2007, Alberta became the first province in Canada to introduce cystic fibrosis (CF) to its newborn screening program. The Alberta protocol involves a two-tier algorithm involving an immunoreactive trypsinogen measurement followed by molecular analysis using a CF panel for 39 mutations. Positive screens are followed up with sweat chloride testing and an assessment by a CF specialist. Of the 99,408 newborns screened in Alberta during the first two years of the program, 221 had a positive CF newborn screen. The program subsequently identified and initiated treatment in 31 newborns with CF. A relatively high frequency of the R117H mutation and the M1101K mutation was noted. The M1101K mutation is common in the Hutterite population. The presence of the R117H mutation has created both counselling and management dilemmas. The ability to offer CF transmembrane regulator full sequencing may help resolve diagnostic dilemmas. Counselling and management challenges are created when mutations are mild or of unknown clinical significance.

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عنوان ژورنال:
  • Paediatrics & child health

دوره 15 9  شماره 

صفحات  -

تاریخ انتشار 2010