| Literature DB >> 36267868 |
Maya Dattatraya Bhat1, Netravathi Manjunath2, Renu Kumari3, Mohammed Faruq4, Pramod Kumar Pal2, Chandrajit Prasad1, Ravindranadh Chowdary Mundlamuri2, Atchayaram Nalini2, Gautham Arunachal Udupi5, Priyanka Priyadarshini Baishya1, Karthik Kulanthaivelu1.
Abstract
Cribriform appearance of the brain in Canavan disease is a rare finding. The two presented cases broaden the magnetic resonance imaging (MRI) phenotype wherein numerous oval, cystic structures, a few resembling dilated Virchow-Robin (VR) spaces, were noted in the centrum semiovale, periventricular, and lobar white matter producing a cribriform pattern. Besides, discrete round to oval cysts were present at the gray-white matter junctions in the second case, which were larger and appeared morphologically distinct from the VR spaces. These cysts did not elongate in any plane on imaging and were more representative of giant intramyelinic vacuoles. Genetic analysis revealed novel mutations in the aspartoacylase or ASPA gene that possibly accounts for the severe form of Canavan disease, which probably explains the imaging findings. The multicystic appearance of the white matter in Canavan disease is unusual and possibly represents two different histopathological substrates. Thieme. All rights reserved.Entities:
Keywords: Canavan disease; cribriform; novel mutation
Year: 2021 PMID: 36267868 PMCID: PMC9578778 DOI: 10.1055/s-0041-1725118
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X