| Literature DB >> 23857099 |
Hiroshi Doi1, Chihiro Ohba, Yoshinori Tsurusaki, Satoko Miyatake, Noriko Miyake, Hirotomo Saitsu, Yuko Kawamoto, Tamaki Yoshida, Shigeru Koyano, Yume Suzuki, Yoshiyuki Kuroiwa, Fumiaki Tanaka, Naomichi Matsumoto.
Abstract
Autosomal recessive cerebellar ataxias and autosomal recessive hereditary spastic paraplegias are clinically and genetically heterogeneous disorders with diverse neurological and non-neurological features. We herein describe a Japanese patient with a slowly progressive form of ataxia and spastic paraplegia. Using whole exome sequencing, we identified a novel homozygous frameshift mutation in SPG7, encoding paraplegin, in this patient. This is the first report of an SPG7 mutation in the Japanese population. For disorders previously undetected in a particular population, or unrecognized/atypical phenotypes, exome sequencing may facilitate molecular diagnosis.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23857099 DOI: 10.2169/internalmedicine.52.0252
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271