Yilmaz Agladioglu S, Aycan Z, Bas V N, Peltek Kendirci H N, Onder A
Dr. Sami Ulus Training and Research Children's Hospital, Clinics of Pediatric Endocrinology, Ankara, Turkey.
Genet Couns. 2012;23(2):149-56.
The thiamine-responsive megaloblastic anemia syndrome (TRMA) is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural hearing loss due to mutations in SLC 19A2 that encodes a thiamine transporter protein. The disease can manifest at any time between infancy and adolescence, and not all cardinal findings are present initially. The anemia typically improves significantly with pharmacological doses of thiamine. Variable improvement in diabetes is also noted. However, the hearing loss is apparently irreversible, although a delay in the onset of deafness may be possible. We present a 2-year old girl with non-autoimmune diabetes mellitus and anemia in whom we found a novelc.95T>A (leu32X) mutation in the SLC19A2 gene in this study.Our patient with this new mutation did not suffer from hearing loss.
硫胺素反应性巨幼细胞贫血综合征(TRMA)是一种常染色体隐性疾病,其特征为糖尿病、巨幼细胞贫血以及由于编码硫胺素转运蛋白的SLC 19A2基因突变所致的感音神经性听力丧失。该疾病可在婴儿期至青春期之间的任何时间出现,且并非所有主要症状最初都会出现。贫血通常在给予药理剂量的硫胺素后会显著改善。糖尿病也有不同程度的改善。然而,听力丧失显然是不可逆的,尽管耳聋的发作可能会延迟。在本研究中,我们报告了一名患有非自身免疫性糖尿病和贫血的2岁女孩,我们在其SLC19A2基因中发现了一个新的c.95T>A(leu32X)突变。我们这位携带新突变的患者未患有听力丧失。