NHEJ1 Splice Variants Associated With Bone Marrow Failure and Hematologic Malignancy

Nonhomologous end-joining (NHEJ)1 deficiency causes a genome maintenance disorder (GMD), classically associated with severe combined immunodeficiency. Here, we describe two cases of NHEJ1 deficiency presenting with cytopenias. One patient was an adolescent with recurrent cytopenias and frank immunodeficiency that evolved into bone marrow failure with myelodysplasia, then chronic myelomonocytic leukemia and ultimately treatment-refractory acute myeloid leukemia. The second patient was a preadolescent with only cytopenias. In both cases, diagnosis was not achieved by sending an inherited BMF syndrome panel because of the omission of NHEJ1. Our cases further emphasize that NHEJ1 deficiency harbors additionally under-recognized hematopoietic implications beyond lymphoid abnormalities, adding to the emerging evidence for coexistent myeloid and lymphoid concerns in GMDs.

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Journal
Pediatric Blood & Cancer
Published
2025-06-28
DOI
https://doi.org/10.1002/pbc.31884
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
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article

NHEJ1 Splice Variants Associated With Bone Marrow Failure and Hematologic Malignancy

Christopher Gamper, Nadav I. Weinstock, Xiao Peng, Jennifer Keates‐Baleeiro et al.
Pediatric Blood & Cancer
Immunodeficiency and Autoimmune Disorders
article

NHEJ1 Splice Variants Associated With Bone Marrow Failure and Hematologic Malignancy

Christopher Gamper, Nadav I. Weinstock, Xiao Peng, Jennifer Keates‐Baleeiro, Carolyn Applegate, Lei Peng
article en

Abstract

Nonhomologous end-joining (NHEJ)1 deficiency causes a genome maintenance disorder (GMD), classically associated with severe combined immunodeficiency. Here, we describe two cases of NHEJ1 deficiency presenting with cytopenias. One patient was an adolescent with recurrent cytopenias and frank immunodeficiency that evolved into bone marrow failure with myelodysplasia, then chronic myelomonocytic leukemia and ultimately treatment-refractory acute myeloid leukemia. The second patient was a preadolescent with only cytopenias. In both cases, diagnosis was not achieved by sending an inherited BMF syndrome panel because of the omission of NHEJ1. Our cases further emphasize that NHEJ1 deficiency harbors additionally under-recognized hematopoietic implications beyond lymphoid abnormalities, adding to the emerging evidence for coexistent myeloid and lymphoid concerns in GMDs.

Pediatric Blood & CancerVol. 72(9)
Albert Einstein College of Medicine (US), Montefiore Medical Center (US), Johns Hopkins Hospital (US)
Good health and well-being
Openalex Percentile: Top 83%
Immunodeficiency and Autoimmune Disorders
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NHEJ1 Splice Variants Associated With Bone Marrow Failure and Hematologic Malignancy — Christopher Gamper, Nadav I. Weinstock, et al. · Pediatric Blood & Cancer (2025) | TGRS Research Map | TGRS