Langerhans cell histiocytosis (LCH) is a rare clonal myeloid neoplasm. Canadian data on clinical characteristics, molecular profile, and treatment outcomes is limited. This study aims to report the initial experience of a Canadian rare diseases program, reflecting “real‐world” diagnostic pathways, referral patterns, an...
S. Quon, Yaswanta K Gummadi, Ibrahim Elsharawi et al.· Hematological Oncology· 0 citations
The Myeloid Malignancy Variant Curation Expert Panel (MM-VCEP) defined GATA2 deficiency as any of the 2,903 combinations of two or three phenotypes with log10Odds Ratio ≥3 (OR ≥ 1000).
S. Mohan, Tilda E Carlelycke, Ashwin L Koppayi et al.· Blood· 0 citations
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