Early Diagnosis and Treatment of Purine Nucleoside Phosphorylase (PNP) Deficiency through TREC-Based Newborn Screening

Int J Neonatal Screen. 2021 Sep 29;7(4):62. doi: 10.3390/ijns7040062.

Abstract

Purine nucleoside phosphorylase (PNP) deficiency is a rare inherited disorder, resulting in severe combined immunodeficiency. To date, PNP deficiency has been detected in newborn screening only through the use of liquid chromatography tandem mass spectrometry. We report the first case in which PNP deficiency was detected by TREC analysis.

Keywords: T-cell receptor excision circle; newborn screening; purine nucleoside phosphorylase deficiency; severe combined immunodeficiency.

Publication types

  • Case Reports