| Literature DB >> 31493991 |
Limin Li1, Choong Yi Fong1, Chee Geap Tay1, Sok Kun Tae1, Hisato Suzuki2, Kenjiro Kosaki2, Meow-Keong Thong3.
Abstract
Infantile neuroaxonal dystrophy 1 (INAD) (OMIM #256600) is a rare infantile onset neurodegenerative disease characterised by neuroregression and hypotonia, evolving into generalized spasticity, blindness and dementia. We report our diagnostic approach of a pair of siblings with psychomotor regression, hypotonia, optic atrophy and auditory neuropathy. The brain magnetic resonance imaging (MRI) showed progressive cerebellar atrophy. Genetic testing of the PLA2G6 confirmed presence of compound heterozygous novel mutations. As the variant c. 196C>T (p.Gln66X) was a truncating variant, it was considered as pathogenic while the variant c. 2249G>A (p. Cys750Tyr) was considered as "likely pathogenic" by bioinformatics analyses. Our patient expands the clinical phenotype of INAD as it described the first South-East Asian patient with INAD-associated auditory neuropathy. Our report highlights the importance of increased awareness of this condition amongst clinicians, the use of deep phenotyping using neuroimaging and the clinical utility of gene sequencing test in the delineation of syndromes associated with infantile neurodegenerative disease.Entities:
Keywords: Auditory neuropathy; Cerebellar atrophy; Infantile neuroaxonal dystrophy; Novel mutation
Mesh:
Substances:
Year: 2019 PMID: 31493991 DOI: 10.1016/j.jocn.2019.08.111
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961