
A NOVEL LIKELY PATHOGENIC VARIANT
IN THE RUNX1 GENE AS THE CAUSE
OF CONGENITAL THROMBOCYTOPENIA Despotović M1,*, Pereza N2, Peterlin B3, Ostojić S2, Golob B3, Maver A3, Roganović J4 *Corresponding Author: Marta Despotović, University of Rijeka, Faculty of Medicine, Braće Branchetta
20, 51000 Rijeka, Croatia. Tel: +385-91-732-6486. E-mail: despotovicmarta@gmail.com page: 4
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CONCLUSION
To the best of our knowledge, the heterozygous
frameshift c.1160delG variant in the RUNX1 gene was
first described in our patient. This sequence variant is the
third described pathogenic or likely pathogenic variant
in exon 9. Although pathogenic variants in the RUNX1
genes are very rare, persistently low platelet counts of
unclear etiology should raise suspicion of an underlying
genetic disorder.
Declaration of Interest. The authors report no conflicts
of interest. The authors alone are responsible for the
content and writing of this article
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