S. van der Crabben, E. van Binsbergen, M. Ausems, M. Poot, M. Bierings and A. Buijs, “Constitutional RUNX1 Deletion Presenting as Non-Syndromic Thrombocytopenia with Myelodysplasia: 21q22 ITSN1 as a Candidate Gene in Mental Retardation,” Leukemia Research, Vol. 34, No. 1, 2010, pp. e8-e12. doi:10.1016/j.leukres.2009.06.030

has been cited by the following article:

• TITLE: Hereditary Leukemia Due to Rare RUNX1c Splice Variant (L472X) Presents with Eczematous Phenotype

  AUTHORS: April Sorrell, Carin Espenschied, Wei Wang, Jeffrey Weitzel, Su Chu, Pablo Parker, Juan-Sebastian Saldivar, Ravi Bhatia

  KEYWORDS: Hereditary Leukemia; Eczema; FPDMM; L472X; RUNX1c Isoform

  JOURNAL NAME: International Journal of Clinical Medicine, Vol.3 No.7, December 31, 2012

  ABSTRACT: Deleterious mutations in the RUNX1 gene cause hereditary leukemia due to a rare syndrome called Familial platelet Disorder with Associated Myeloid Malignancy (FPDMM). We describe the characteristics of a family with FPDMM due to a novel RUNX1 mutation (L472X), located in the most 3-prime end of the gene reported to date. Our 36-year-old proband presented with incidentally detected thrombocytopenia and a family history suggestive of FPDMM. Contrary to previously described families, affected members of our kindred express an eczematous phenotype, reportedly most severe in members who develop leukemia. Pedigree analysis shows that the L472X mutation tracks with thrombocytopenia, acute leukemia, and eczema. The L472X mutation produces a stably expressed RUNX1 protein product with a corresponding decrease in wild type RUNX1 expression. Our data supports the inclusion of eczema in the FPDMM phenotype and suggests the possibility that the RUNX1 L472X mutant causes the type of dominant negative affect that is associated with an elevated risk of leukemia in FPDMM families.