Literature DB >> 26371980

A novel AMT gene mutation in a newborn with nonketotic hyperglycinemia and early myoclonic encephalopathy.

Vincenzo Belcastro1, Mario Barbarini2, Salvatore Barca3, Isabella Mauro2.   

Abstract

Early myoclonic encephalopathy (EME) presents in neonatal period with erratic or fragmentary myoclonus and a burst-suppression electroencephalography (EEG) pattern. Nonketotic hyperglycinemia (NKH) is the most common metabolic cause of EME and genetic testing confirms the diagnosis of NKH in around 75% of the patients with a clinical diagnosis of NKH. Three genes are known to cause NKH. Here we describe a case of EME caused by NKH in which a new mutation in aminomethyltransferase (AMT) gene has been detected.
Copyright © 2015 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  AMT gene mutations; Burst-suppression; Early myoclonic encephalopathy; Massive myoclonus; Nonketotic hyperglycinemia; Tonic spasms

Mesh:

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Year:  2015        PMID: 26371980     DOI: 10.1016/j.ejpn.2015.08.008

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  2 in total

1.  [Clinical and molecular genetic characteristics of nonketotic hyperglycinemia].

Authors:  Hai-Feng Li
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2017-03

Review 2.  Epilepsy in inherited neurotransmitter disorders: Spotlights on pathophysiology and clinical management.

Authors:  Mario Mastrangelo
Journal:  Metab Brain Dis       Date:  2020-10-23       Impact factor: 3.584

  2 in total

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