Thiamine-responsive megaloblastic anemia syndrome: A case report

Thiamine-responsive megaloblastic anemia syndrome: A case report

Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare autosomal recessive disorder characterized by a cardinal triad consisting of megaloblastic anemia, sensorineural deafness, and diabetes mellitus. TRMA is caused by mutations in the gene SLC19A2 encoding a high-affinity thiamine trans...

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Bibliographic Details
Main Authors: Omkar Patil, Karnam Guruswamy Ravikumar, Sundaramoorthy Gopi, Thulasi Raman, Venkatesan Radha, Viswanathan Mohan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Journal of Diabetology
Subjects:
diabetes mellitus
slc19a2 gene
thiamine-responsive megaloblastic anemia
trma
Online Access:http://www.journalofdiabetology.org/article.asp?issn=2078-7685;year=2020;volume=11;issue=1;spage=45;epage=48;aulast=Patil

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http://www.journalofdiabetology.org/article.asp?issn=2078-7685;year=2020;volume=11;issue=1;spage=45;epage=48;aulast=Patil

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