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International Journal of Neonatal Screening, Volume 5, Issue 2

June 2019 - 8 articles

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Articles (8)

  • Article
  • Open Access
58 Citations
5,990 Views
12 Pages

Implementation of Second-Tier Tests in Newborn Screening for Lysosomal Disorders in North Eastern Italy

  • Alberto B. Burlina,
  • Giulia Polo,
  • Laura Rubert,
  • Daniela Gueraldi,
  • Chiara Cazzorla,
  • Giovanni Duro,
  • Leonardo Salviati and
  • Alessandro P. Burlina

The increasing availability of treatments and the importance of early intervention have stimulated interest in newborn screening for lysosomal storage diseases. Since 2015, 112,446 newborns in North Eastern Italy have been screened for four lysosomal...

  • Article
  • Open Access
41 Citations
5,906 Views
14 Pages

Genetic results of uncertain clinical significance are being returned to parents following newborn screening, representing a paradigm change in how society considers health and illness. ‘Cystic Fibrosis screen positive, inconclusive diagnosis&r...

  • Review
  • Open Access
12 Citations
6,507 Views
10 Pages

A Newborn Screening Education Best Practices Framework: Development and Adoption

  • Adrianna Evans,
  • Keri LeBlanc,
  • Natasha Bonhomme,
  • Scott M. Shone,
  • Amy Gaviglio,
  • Debra Freedenberg,
  • Jeremy Penn,
  • Carol Johnson,
  • Beth Vogel and
  • Siobhan M. Dolan
  • + 1 author

Newborn screening is a process-based public health service. Newborn screening staff and families alike are essential to maintaining the timeliness of the screening process. Newborn screening education must be accurate and accessible. Past newborn scr...

  • Article
  • Open Access
15 Citations
6,783 Views
9 Pages

Validation of a Fast, Robust, Inexpensive, Two-Tiered Neonatal Screening Test algorithm on Dried Blood Spots for Spinal Muscular Atrophy

  • Annuska Strunk,
  • Andre Abbes,
  • Antoine R. Stuitje,
  • Chris Hettinga,
  • Eline M. Sepers,
  • Reinier Snetselaar,
  • Jan Schouten,
  • Fay-Lynn Asselman,
  • Inge Cuppen and
  • Henny Lemmink
  • + 2 authors

Spinal muscular atrophy (SMA) is one of the leading genetic causes of infant mortality with an incidence of 1:10,000. The recently-introduced antisense oligonucleotide treatment improves the outcome of this disease, in particular when applied at an e...

  • Review
  • Open Access
162 Citations
65,546 Views
15 Pages

Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment

  • Baba P. D. Inusa,
  • Lewis L. Hsu,
  • Neeraj Kohli,
  • Anissa Patel,
  • Kilali Ominu-Evbota,
  • Kofi A. Anie and
  • Wale Atoyebi

Sickle cell disease (SCD) is a monogenetic disorder due to a single base-pair point mutation in the β-globin gene resulting in the substitution of the amino acid valine for glutamic acid in the β-globin chain. Phenotypic variation in the clinical pre...

  • Article
  • Open Access
10 Citations
6,734 Views
11 Pages

Galactosaemia has been included in various newborn screening programs since 1963. Several methods are used for screening; however, the predominant methods used today are based on the determination of either galactose-1-phosphate uridyltransferase (GA...

  • Article
  • Open Access
11 Citations
6,136 Views
12 Pages

Newborn Screening for Selected Disorders in Nepal: A Pilot Study

  • Arti Sharma Pandey,
  • Suchita Joshi,
  • Rateena Rajbhandari,
  • Prerana Kansakar,
  • Sadichhya Dhakal and
  • Ralph Fingerhut

The prevalence of metabolic disorders in Nepal is yet unknown, although many case reports occur in literature. Heel-prick blood samples from newborns were collected on Dried Blood Spot (DBS) collection cards and tested through Tandem Mass Spectroscop...

  • Article
  • Open Access
9 Citations
4,245 Views
12 Pages

For newborn screening (NBS) of lysosomal storage diseases, programs measure enzymatic activities in dried blood spots (DBS) and, in most cases, act on samples where the measurement is below a specific cutoff value. The rate of false positives and neg...

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Int. J. Neonatal Screen. - ISSN 2409-515X