Literature DB >> 31361176

ZRSR2 mutation in a child with refractory macrocytic anemia and Down Syndrome.

Meghna Srinath1, Emily Coberly2, Kimberly Ebersol3, Kirstin Binz1, Katsiaryna Laziuk2, William T Gunning4, Barbara Gruner3, Richard Hammer2, Bindu Kanathezhath Sathi3.   

Abstract

Here we report a case of refractory macrocytic anemia with a spliceosomal point mutation involving the ZRSR2 gene in a child with Down syndrome (DS). Such mutations have been shown to cause refractory macrocytic anemia and myelodysplastic syndrome (MDS) in elderly individuals. We report the hematological indices of a child with DS and a ZRSR2 spliceosomal mutation. DS is known to produce macrocytic anemia but does not lead to transfusion dependence. In this case, the ZRSR2 mutation was the likely implicating factor for severe transfusion-dependent anemia in a child with DS. The clinical implication of a ZRSR2 mutation in a child with DS has not been previously described and warrants close surveillance to detect potential insidious transformation to MDS.

Entities:  

Keywords:  Down syndrome; myelodysplastic syndrome; refractory macrocytic anemia; spliceosomal mutation

Year:  2019        PMID: 31361176     DOI: 10.1080/08880018.2019.1621969

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  1 in total

1.  Zrsr2 Is Essential for the Embryonic Development and Splicing of Minor Introns in RNA and Protein Processing Genes in Zebrafish.

Authors:  Rachel Weinstein; Kevin Bishop; Elizabeth Broadbridge; Kai Yu; Blake Carrington; Abdel Elkahloun; Tao Zhen; Wuhong Pei; Shawn M Burgess; Paul Liu; Erica Bresciani; Raman Sood
Journal:  Int J Mol Sci       Date:  2022-09-14       Impact factor: 6.208

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.