Title : Thiamine responsive megaloblastic anemia syndrome.

Pub. Date : 2009 Mar

PMID : 19347672






4 Functional Relationships(s)
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1 Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness. Thiamine solute carrier family 19 member 2 Homo sapiens
2 Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness. Thiamine solute carrier family 19 member 2 Homo sapiens
3 We report a 4-year-old girl with TRMA whose anemia improved following administration of thiamine and this case report sensitizes the early diagnosis and treatment with thiamine in children presenting with anemia, diabetes and deafness. Thiamine solute carrier family 19 member 2 Homo sapiens
4 We report a 4-year-old girl with TRMA whose anemia improved following administration of thiamine and this case report sensitizes the early diagnosis and treatment with thiamine in children presenting with anemia, diabetes and deafness. Thiamine solute carrier family 19 member 2 Homo sapiens