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J Hum Genet. 2017 Feb;62(2):329-333. doi: 10.1038/jhg.2016.126. Epub 2016 Oct 13.

Novel AARS2 gene mutation producing leukodystrophy: a case report.

Author information

1
Department of Neurology, University of Szeged, Szeged, Hungary.
2
Department of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
3
MTA-SZTE Neuroscience Research Group, Szeged, Hungary.
4
Institute of Neurology, Medical University of Vienna, Vienna, Austria.

Abstract

AARS2 gene (NM_020745.3) mutations result in two different phenotypic diseases: infantile mitochondrial cardiomyopathy and late-onset leukoencephalopathy. The patient's first symptoms appeared at the age of 18 years with behavioral changes and psychiatric problems. Some years later, extrapyramidal symptoms, cognitive impairment, nystagmus, dysarthria and pyramidal symptoms also developed. The brain magnetic resonance imaging (MRI) indicated extensive white matter abnormalities. The diagnosis of AARS2 gene mutations causing leukodystrophy was confirmed by genetic testing. Segregation analysis confirmed the compound heterozygous state of the patient. Histological examination of the biopsy did not prove specific pathological alterations. The clinical phenotype of our patient was compared with seven previously described patients suffering from leukoencephalopathy caused by AARS2 mutations. We have documented a new, nonsense AARS2 gene mutation (c.578T>G, p.Leu193*) and a known missense mutation (c.595C>T, p.Arg199Cys) associated with leukoencephalopathy in a male patient. Clinical features, imaging characteristics and genetic testing are presented, and histological data from an AARS2-related leukodystrophy patient are described for the first time.

PMID:
27734837
DOI:
10.1038/jhg.2016.126
[Indexed for MEDLINE]

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