Leukocytosis and Splenomegaly in a Neonate With NRAS Mutation

Clin Pediatr (Phila). 2024 May;63(4):451-455. doi: 10.1177/00099228231176341. Epub 2023 Jun 1.

Authors

Michelle H Lucena¹, Palanikumar Balasundaram¹, Megan Carney², Erica Green², Margo S Breilyn³, Mamta Fuloria¹

Affiliations

¹ Division of Neonatology, Department of Pediatrics, The Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA.
² Department of Pediatrics, The Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA.
³ Division of Medical Genetics and Genomics, Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

PMID: 37264612
DOI: 10.1177/00099228231176341

No abstract available

MeSH terms

GTP Phosphohydrolases / genetics
Humans
Infant, Newborn
Leukocytosis* / genetics
Membrane Proteins / genetics
Mutation
Splenomegaly* / genetics

Substances

GTP Phosphohydrolases
Membrane Proteins
NRAS protein, human