Skip to main content
Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs).
- Author(s): Patel, Jay P
- Puck, Jennifer M
- Srinivasan, Rajgopal
- Brown, Christina
- Sunderam, Uma
- Kundu, Kunal
- Brenner, Steven E
- Gatti, Richard A
- Church, Joseph A
- et al.
Published Web Locationhttp://ucelinks.cdlib.org:8888/sfx_local?issn=0271-9142&id=doi:10.1007/s10875-015-0136-6&spage=227&volume=35&issue=2&date=2015
No data is associated with this publication.
PurposeSevere combined immunodeficiency (SCID) encompasses a group of disorders characterized by reduced or absent T-cell number and function and identified by newborn screening utilizing T-cell receptor excision circles (TRECs). This screening has also identified infants with T lymphopenia who lack mutations in typical SCID genes. We report an infant with low TRECs and non-SCID T lymphopenia, who proved upon whole exome sequencing to have Nijmegen breakage syndrome (NBS).
MethodsExome sequencing of DNA from the infant and his parents was performed. Genomic analysis revealed deleterious variants in the NBN gene. Confirmatory testing included Sanger sequencing and immunoblotting and radiosensitivity testing of patient lymphocytes.
ResultsTwo novel nonsense mutations in NBN were identified in genomic DNA from the family. Immunoblotting showed absence of nibrin protein. A colony survival assay demonstrated radiosensitivity comparable to patients with ataxia telangiectasia.
ConclusionsAlthough TREC screening was developed to identify newborns with SCID, it has also identified T lymphopenic disorders that may not otherwise be diagnosed until later in life. Timely identification of an infant with T lymphopenia allowed for prompt pursuit of underlying etiology, making possible a diagnosis of NBS, genetic counseling, and early intervention to minimize complications.
Item not freely available? Link broken?Report a problem accessing this item