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...

Full description

Saved in:
Bibliographic Details
Main Authors: Karimzadeh, Parvaneh, Moosavian, Toktam, Moosavian, Hamidreza
Format: Online
Published: Iranian Journal of Child Neurology 2017
Online Access:

CIC - Centro de Información y Conocimiento Johannes Gutenberg ®