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Thiamine transport by erythrocytes and ghosts in thiamine-responsive megaloblastic anaemia

โœ Scribed by G. Rindi; D. Casirola; V. Poggi; B. De Vizia; C. Patrini; U. Laforenza

Publisher
Springer
Year
1992
Tongue
English
Weight
923 KB
Volume
15
Category
Article
ISSN
0141-8955

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Thiamine responsive megaloblastic anemia (TRMA) is an autosomal recessive disorder with a triad of symptoms: megaloblastic anemia, deafness, and non-type 1 diabetes mellitus. Occasionally, cardiac abnormalities and abnormalities of the optic nerve and retina occur as well. Patients with TRMA often r