| Literature DB >> 27882168 |
Haifeng Li1, Yan Zou2, Xinhua Bao3, Hui Wang1, Jiangping Wang1, Huiying Jin1, Yuping Che1, Xiaoyan Tang4.
Abstract
Infantile neuroaxonal dystrophy (INAD) is a rare neurodegenerative disease with early onset. PLA2G6 gene mutations have been identified in the majority individuals with INAD. In future, molecular diagnosis of INAD will replace the invasive biopsies used previously. In the present report, monozygotic male twins with INAD were referred The Children's Hospital (Zhejiang University School of Medicine, Zhejiang, China) at fifteen months old for delayed development. The older brother was found to have developmental stagnation when he was 6 months old. The patient could not stand securely without support, and had poor eye tracking and listening ability. Magnetic resonance imaging (MRI) of the patient's brain revealed cerebellar atrophy and electromyography identified signs of peripheral neuropathy. The younger brother displayed similar clinical features and findings. Two different phospholipase A2 group VI (PLA2G6; 22q13.1) gene mutations were detected in the twins by DNA sequencing. The results of the present study indicate that neurogenetic disease should be considered when child patients present with idiopathic developmental stagnation, particularly when similar cases have appeared in the same family. In addition, INAD should be considered as a possible diagnosis when the patient has developmental delay of the central and peripheral nerves. In the future, molecular genetic testing will be the primary method of INAD diagnosis, enabling better prevention of this genetic disease.Entities:
Keywords: infantile neuroaxonal dystrophy; magnetic resonance imaging; phospholipase A2 group VI
Year: 2016 PMID: 27882168 PMCID: PMC5103811 DOI: 10.3892/etm.2016.3761
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447