Recurrent stroke in a child with TRMA syndrome and SLC19A2 gene mutation
Here we report a 5-month-old boy with thiamine Responsive Megaloblastic Anemia syndrome (TRMA syndrome) with several attacks of stroke. In addition to the cardinal clinical manifestations of the syndrome (thiamine-responsive megaloblastic anemia, diabetes mellitus, and sensor neural hearing loss), t...
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Iranian Journal of Child Neurology