Roger Syndrome Case Report
Keywords:
Roger syndrome
Abstract
Roger syndrome (Thiamin Responsive Megaloblastic Anemia Syndrome), is characterized by megaloblastic anemia, deafness and diabetes mellitus. It is an autosomal recessive disorder due to mutation in SLC 19A2 gene that leads to defective thiamine transport protein. So, thiamine is not absorbed and effectively utilized by body from diet.
Published
2020-07-02
How to Cite
Ayesha, H., Taseer, A., & Khan, M. (2020). Roger Syndrome Case Report. Annals of Punjab Medical College, 14(1), 97-98. https://doi.org/10.29054/apmc/2020.716
Section
Case Reports