A Thiamine Responsive Megaloblastic Anemia Presented with Hypertriglyceridemia and Auto-immune Diabetes

Abstract Abstract Background: Thiamine responsive megaloblastic anemia syndrome (TRMA) is an autosomal recessive disorder characterized by non type 1 diabetes mellitus (DM), sensorineural hearing loss and megaloblastic anemia and caused by mutations in SLC19A2 gene, encoding a thiamine transporter p...

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Veröffentlicht in:	Experimental and clinical endocrinology & diabetes reports 2017-02, Vol.2 (1), p.e8-e10
Hauptverfasser:	Yılmaz, Y., Aydın, B. K., Baş, F., Ünüvar, A., Karakaş, Z., Poyrazoğlu, Ş., Bundak, R., Darendeliler, F.
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report
Online-Zugang:	Volltext
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