Evaluation of MYORG mutations as a novel cause of primary familial brain calcification

• Published in: Movement disorders Vol. 34; no. 2; pp. 291 - 297
• Main Authors: Chen, You, Fu, Feng, Chen, Si, Cen, Zhidong, Tang, Haiyan, Huang, Jinxiu, Xie, Fei, Zheng, Xiaosheng, Yang, Dehao, Wang, Haotian, Huang, Xuerong, Zhang, Yun, Zhou, Yongji, Liu, Jing‐Yu, Luo, Wei
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.02.2019
• Subjects: Adult; Basal ganglia; Basal Ganglia - pathology; Brain Diseases - genetics; Calcification; Calcinosis - genetics; Cerebellum; China; Cognitive ability; Cohort Studies; DNA Mutational Analysis - methods; Female; Founder effect; Glycoside Hydrolases - genetics; Haplotypes; Heredity; Heterozygote; Humans; Insertion; Male; Missense mutation; Movement disorders; Mutation; Mutation - genetics; mutations; MYORG; Neurodegenerative Diseases - genetics; Nonsense mutation; Pedigree; primary familial brain calcification; Sodium-Phosphate Cotransporter Proteins, Type III - genetics; Substantia alba; Thalamus; China; primary familial brain calcification; mutations; founder effect; MYORG
• ISSN: 0885-3185; 1531-8257
• DOI: 10.1002/mds.27582

ABSTRACT Background Very recently, the MYORG gene was identified as a novel causative gene for autosomal‐recessive primary familial brain calcification. Objective To investigate the clinical, genetic, and neuroradiological characteristics of primary familial brain calcification patients with biallelic MYORG mutations in China. Methods We collected clinical and neuroradiological data of 169 Chinese patients with primary familial brain calcification, including 151 sporadic patients and 18 patients from 13 families compatible with an autosomal‐recessive mode of inheritance. Mutational analysis of MYORG was performed in the cohort. Results We identified four, including three novel, MYORG mutations segregating in four families with 5 patients: one nonsense mutation (c.1431C>A, p.Y477*), one missense mutation (c.687G>T, p.W229C), and two nonframeshift indels (c.348_349insCTGGCCTTCCGC, p.116_117insLAFR; c. 428_442delTGCACTTCTTCATCC, p.143_147delLHFFI). The 12‐base‐pair insertion, c.348_349insCTGGCCTTCCGC, was found in either homozygous or heterozygous state in 2 probands of our cohort and another Chinese primary familial brain calcification patient previously reported on in the literature. Haplotype analysis of our patients harboring the insertion indicated a founder effect in the ethnic Han Chinese population. To date, biallelic MYORG mutations have been reported in 17 patients (including our cohort). Most patients were symptomatic (13 of 17; 76.5%), and the most recurrent symptoms were movement disorders (10 of 17; 58.8%), cognitive decline (7 of 17; 41.2%), and cerebellar symptoms (6 of 17; 35.3%). All patients had calcifications on comprehensive cranial CT, most frequently located in the basal ganglia (17 of 17; 100%), cerebellum (17 of 17; 100%), subcortical white matter (14 of 17; 82.4%), and thalamus (13 of 17; 76.5%). Conclusions We confirmed MYORG as a novel causative gene for primary familial brain calcification and further expanded the mutational and phenotypic spectrum of MYORG‐related primary familial brain calcification. © 2018 International Parkinson and Movement Disorder Society