Putative new childhood leukemia cancer predisposition syndrome caused by germline bi‐allelic missense mutations in DDX41

• Published in: Genes chromosomes & cancer Vol. 57; no. 12; pp. 670 - 674
• Main Authors: Diness, Birgitte R., Risom, Lotte, Frandsen, Thomas L., Hansen, Bente, Andersen, Mette K., Schmiegelow, Kjeld, Wadt, Karin A. W.
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.12.2018
• Subjects: Acute myeloid leukemia; Bone marrow; BPDCN; Cancer; cancer predisposition; Child, Preschool; Children; DDX41; DEAD-box RNA Helicases - genetics; Dendritic Cells; Developmental Disabilities - complications; Developmental Disabilities - genetics; Exome; Female; Genetic Predisposition to Disease; germline; Health risks; Heterozygotes; Humans; Infant, Newborn; Leukemia; Leukemia, Myeloid - complications; Leukemia, Myeloid - genetics; Missense mutation; Mutation; Mutation, Missense; Myelodysplastic syndrome; Myeloid leukemia; Pedigree; Pregnancy; Psychomotor Disorders - complications; Psychomotor Disorders - genetics; Ribonucleic acid; RNA; Sarcoidosis; Siblings; Syndrome; cancer predisposition; DDX41; germline; BPDCN
• ISSN: 1045-2257; 1098-2264
• DOI: 10.1002/gcc.22680

DDX41 has recently been identified as a new autosomal dominantly inherited cancer predisposition syndrome causing increased risk of adult onset acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). We report for the first time compound heterozygote germline missense DDX41 mutations located in the DEAD‐box domain, identified in two siblings by exome sequencing. Both siblings have slight dysmorphic findings, psychomotor delays and intellectual disability, and one developed blastic plasmacytoid dendritic cell neoplasm (BPDCN) at age five. RNA‐sequencing of bone marrow showed DDX41 expression including both mutations. However, the allele fraction of p.Pro321Leu accounted for 96% in the RNA‐sequencing indicating this mutation to be the more significant variant. Exome sequencing of the leukemic blasts identified no additional known driver mutations. There is no pattern indicating autosomal dominantly inherited cancer predisposition in the family, but the father has sarcoidosis, which has been associated with heterozygous DDX41 mutation. We propose that bi‐allelic mutations in DDX41 could potentially be a new cancer predisposition syndrome associated with delayed psychomotor development.