Literature DB >> 31243025

Neonatal diabetes mellitus: remission induced by novel therapy.

Pradip Dalwadi1, Ameya S Joshi1, Darshana Sudip Thakur1, Nikhil M Bhagwat1.   

Abstract

A female child with deafness was diagnosed to have neonatal diabetes mellitus at the age of 6 months, on routine evaluation prior to cochlear implant surgery. She presented to us at 11 months of age with diabetic ketoacidosis due to an intercurrent febrile illness. Her haematological parameters showed megaloblastic anaemia and thrombocytopenia. Therefore a possibility of Thiamine Responsive Megaloblastic Anaemia (TRMA) syndrome was considered. She was empirically treated with parenteral thiamine hydrochloride (Hcl). Subsequently, due to the unavailability of pharmacological preparation of oral thiamine Hcl in a recommended dose she was treated with benfotiamine. She had a sustained improvement in all her haematological parameters on oral benfotiamine. The insulin requirement progressively reduced and she is currently in remission for last 2 years. The genetic analysis confirmed the diagnosis of TRMA syndrome. Thus benfotiamine can be considered a new treatment option in management of TRMA syndrome. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  diabetes; endocrine system; haematology (incl blood transfusion); neonatal and paediatric intensive care; paediatrics (drugs and medicines)

Mesh:

Substances:

Year:  2019        PMID: 31243025      PMCID: PMC6605936          DOI: 10.1136/bcr-2018-228806

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  17 in total

1.  Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.

Authors:  E J Neufeld; H Mandel; T Raz; R Szargel; C N Yandava; A Stagg; S Fauré; T Barrett; N Buist; N Cohen
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

Review 2.  Pharmacokinetics of thiamine derivatives especially of benfotiamine.

Authors:  D Loew
Journal:  Int J Clin Pharmacol Ther       Date:  1996-02       Impact factor: 1.366

3.  Thiamine-responsive megaloblastic anemia.

Authors:  F S Porter; L E Rogers; J B Sidbury
Journal:  J Pediatr       Date:  1969-04       Impact factor: 4.406

4.  Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy.

Authors:  F M Meire; K Lemmens; M H Ens-Dokkum
Journal:  Ophthalmic Genet       Date:  2000-12       Impact factor: 1.803

5.  A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I.

Authors:  C Scharfe; M Hauschild; T Klopstock; A J Janssen; P H Heidemann; T Meitinger; M Jaksch
Journal:  J Med Genet       Date:  2000-09       Impact factor: 6.318

6.  Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts.

Authors:  A R Stagg; J C Fleming; M A Baker; M Sakamoto; N Cohen; E J Neufeld
Journal:  J Clin Invest       Date:  1999-03       Impact factor: 14.808

7.  Thiamine-responsive megaloblastic anemia syndrome: long term follow-up.

Authors:  Caterina Borgna-Pignatti; Milena Azzalli; Stefania Pedretti
Journal:  J Pediatr       Date:  2009-08       Impact factor: 4.406

8.  Defective RNA ribose synthesis in fibroblasts from patients with thiamine-responsive megaloblastic anemia (TRMA).

Authors:  László G Boros; Mara P Steinkamp; Judith C Fleming; Wai-Nang Paul Lee; Marta Cascante; Ellis J Neufeld
Journal:  Blood       Date:  2003-07-31       Impact factor: 22.113

9.  Thiamine responsive anaemia: a study of two further cases.

Authors:  C Haworth; D I Evans; J Mitra; S N Wickramasinghe
Journal:  Br J Haematol       Date:  1982-04       Impact factor: 6.998

10.  Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?

Authors:  Leyla Akın; Selim Kurtoğlu; Mustafa Kendirci; Mustafa Ali Akın; Musa Karakükçü
Journal:  J Clin Res Pediatr Endocrinol       Date:  2011-02-23
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