Literature DB >> 30031565

[Thiamine-responsive megaloblastic anemia or Rogers syndrome: A literature review].

H Lu2, H Lu2, J Vaucher3, C Tran4, P Vollenweider3, J Castioni3.   

Abstract

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. Diagnosis relies on uncovering genetic variations (alleles) in the SLC19A2 gene, encoding for a high affinity thiamine transporter. This transporter is essentially present in hematopoietic stem cells, pancreatic beta cells and inner ear cells, explaining the clinical manifestations of the disease. Based on a multidisciplinary approach, treatment resides on lifelong thiamine oral supplementation at pharmacological doses, which reverses anemia and may delay development of diabetes. However, thiamine supplementation does not alleviate already existing hearing defects.
Copyright © 2018 Société Nationale Française de Médecine Interne (SNFMI). Published by Elsevier Masson SAS. All rights reserved.

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Keywords:  Analyse de mutations d’ADN; Anémie mégaloblastique; Carence en thiamine; DNA mutational analysis; Diabetes mellitus; Diabète; Megaloblastic anemia; Sensorineural hearing loss; Surdité neurosensorielle; Thiamine deficiency

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Year:  2018        PMID: 30031565     DOI: 10.1016/j.revmed.2018.06.005

Source DB:  PubMed          Journal:  Rev Med Interne        ISSN: 0248-8663            Impact factor:   0.728


  1 in total

1.  Case Report: Genetic and Clinical Features of Maternal Uniparental Isodisomy-Induced Thiamine-Responsive Megaloblastic Anemia Syndrome.

Authors:  Pengjiang Kang; Weihua Zhang; Jinquan Wen; Jiming Zhang; Fei Li; Wuxia Sun
Journal:  Front Pediatr       Date:  2021-03-19       Impact factor: 3.418

  1 in total

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