| Literature DB >> 26371980 |
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.Entities:
Keywords: AMT gene mutations; Burst-suppression; Early myoclonic encephalopathy; Massive myoclonus; Nonketotic hyperglycinemia; Tonic spasms
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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