TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys

A new syndrome of diabetes, short stature, microcephaly and intellectual disability has been described in association with mutations in the tRNA methyltransferase 10 homologue A (TRMT10A) gene. We report a patient who presented with fasting hyperglycemia, a raised hemoglobin A1c and positive islet c...

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Main Authors: Eve Stern (Author), Asaf Vivante (Author), Ortal Barel (Author), Yael Levy-Shraga (Author)
Format: Book
Published: Galenos Yayincilik, 2022-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Eve Stern  |e author 
700 1 0 |a Asaf Vivante  |e author 
700 1 0 |a Ortal Barel  |e author 
700 1 0 |a Yael Levy-Shraga  |e author 
245 0 0 |a TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys 
260 |b Galenos Yayincilik,   |c 2022-06-01T00:00:00Z. 
500 |a 10.4274/jcrpe.galenos.2020.2020.0265 
500 |a 1308-5727 
500 |a 1308-5735 
520 |a A new syndrome of diabetes, short stature, microcephaly and intellectual disability has been described in association with mutations in the tRNA methyltransferase 10 homologue A (TRMT10A) gene. We report a patient who presented with fasting hyperglycemia, a raised hemoglobin A1c and positive islet cell autoantibodies. Additional clinical features included intellectual disability, hypoplastic kidneys and short stature. In view of the syndromic features coexistant with diabetes, genetic evaluation was carried out, revealing a homozygous mutation in the TRMT10A gene (c.616G>A, p.G206R). The case highlights the importance of genetic evaluation of patients with diabetes with atypical features that can further progress our understanding of the pathophysiology of the rarer subtypes of diabetes. 
546 |a EN 
690 |a monogenic diabetes 
690 |a short stature 
690 |a microcephaly 
690 |a hypoplastic kidneys 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Diseases of the endocrine glands. Clinical endocrinology 
690 |a RC648-665 
655 7 |a article  |2 local 
786 0 |n JCRPE, Vol 14, Iss 2, Pp 227-232 (2022) 
787 0 |n https://jcrpe.org/jvi.aspx?pdir=jcrpe&plng=eng&un=JCRPE-00710&look4= 
787 0 |n https://doaj.org/toc/1308-5727 
787 0 |n https://doaj.org/toc/1308-5735 
856 4 1 |u https://doaj.org/article/3967adb0e10a43b7ac58ec8e08b056b4  |z Connect to this object online.