Transient abnormal lymphomyelopoiesis in a newborn with PTPN11 mutation associated Noonan syndrome

Cytometry B Clin Cytom. 2022 Sep;102(5):409-411. doi: 10.1002/cyto.b.22087. Epub 2022 Jul 4.

Authors

Eman Abdelghani¹, Clifford Mueller², Huifei Liu³

Affiliations

¹ Department of Hematology/Oncology/BMT, Division of Pediatrics, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, Ohio, USA.
² Department of Neonatology, Division of Pediatrics, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, Ohio, USA.
³ Esoterix Pathology Practice Group, Brentwood, Tennessee, USA.

PMID: 35785469
DOI: 10.1002/cyto.b.22087

No abstract available

Publication types

Letter

MeSH terms

Flow Cytometry
Humans
Infant, Newborn
Mutation / genetics
Noonan Syndrome* / complications
Noonan Syndrome* / diagnosis
Noonan Syndrome* / genetics
Phenotype
Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics

Substances

PTPN11 protein, human
Protein Tyrosine Phosphatase, Non-Receptor Type 11