Optical coherence tomography features in brothers with aspartylglucosaminuria

Ann Clin Transl Neurol. 2018 Oct 24;5(12):1622-1626. doi: 10.1002/acn3.672. eCollection 2018 Dec.

Abstract

Aspartylglucosaminuria is a lysosomal storage disorder enriched in Finland. We report on a pair of non-Finnish siblings with aspartylglucosaminuria with autofluorescent inclusion bodies on optical coherence tomography, a finding not previously reported in this disorder. We performed a record review, neurological and neuropsychological evaluation, brain MRI, and optical coherence tomography for each patient. They are compound heterozygous for a 34-kb deletion and a c.365C>A novel variant of the AGA gene. Autofluorescent inclusion bodies were found on optical coherence tomography in the older, more severely affected brother. We hypothesize the finding represents a noninvasive biomarker of disease severity for aspartylglucosaminuria.

Publication types

  • Case Reports

Grant support

This work was funded by National Multiple Sclerosis Society grant ; Rare Trait Hope Fund grant .