Recurrent Stroke in a Child with TRMA Syndrome and SLC19A2 Gene Mutation
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DOI: 10.22037/ijcn.v12i1.17272
Abstract: Here we report a 5-month-old boy with thiamine Responsive Megaloblastic Anemia syndrome (TRMA syndrome) with several attacks of stroke, admitted to Mofid Children's Hospital, Tehran, Iran, in 2016. In addition to the cardinal clinical manifestations… read more here.
Keywords: mutation; megaloblastic anemia; slc19a2 gene; trma syndrome ... See more keywords