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Thiamine responsive megaloblastic anemia syndrome

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Thiamine responsive megaloblastic anemia syndrome" returned 0 free, full-text review articles. First 0 results:
[Thiamine-responsive megaloblastic anemia or Rogers syndrome: A literature review].
Last Updated: May 28, 2019

Thiamine-responsive megaloblastic anemia (TRMA), also known as Rogers syndrome, is a rare autosomal recessive disease characterized by three main components: megaloblastic anemia, diabetes mellitus and sensorineural deafness. Those features occur in infancy but may arise during adolescence. ...

Cardiac manifestations in thiamine-responsive megaloblastic anemia syndrome.
Last Updated: Nov 13, 2018

Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and sensorineural deafness, responding in varying degrees to thiamine treatment. Other features of this syndrome gradually ...

Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport.
Last Updated: Nov 21, 2013

Thiamine-responsive megaloblastic anemia (TRMA) syndrome (OMIM No. 249270) comprises a distinctive triad of clinical features: megaloblastic anemia with ringed sideroblasts, diabetes mellitus, and progressive sensorineural deafness. The TRMA gene has been mapped and cloned. Designated ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Thiamine responsive megaloblastic anemia syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Thiamine responsive megaloblastic anemia syndrome" returned 6 free, full-text research articles. First few results:
Arrhythmia in thiamine responsive megaloblastic anemia syndrome.
Last Updated: Feb 25, 2019

Argun M, Baykan A, Hatipoğlu N, Akın L, Şahin Y, Narin N, Kurtoğlu S. Arrhythmia in thiamine responsive megaloblastic anemia syndrome. Turk J Pediatr 2018; 60: 348-351. Thiamine responsive megaloblastic anemia syndrome (TRMAS) is a rare, autosomal recessive disorder characterized ...

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.
Last Updated: May 11, 2018

Thiamine-responsive megaloblastic anemia syndrome (TRMA), also known as Rogers syndrome, is characterized by megaloblastic anemia, sensorineural hearing loss, and diabetes mellitus. Disturbances of the thiamine transport into the cells results from homozygous or compound heterozygous ...

Thiamine responsive megaloblastic anemia syndrome: a novel homozygous SLC19A2 gene mutation identified.
Last Updated: Jun 22, 2015

Thiamine responsive megaloblastic anemia syndrome (TRMAS) is a rare autosomal recessive disorder especially in countries where consanguinity is uncommon. Three main features are characteristic of the disease - megaloblastic anemia, early onset deafness, and non-type I diabetes. TRMAS ...

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6 Free Research Articles 19 Research Articles