| Literature DB >> 17726686 |
Randi J Hagerman1, Sarah M Coffey, Ricardo Maselli, Kultida Soontarapornchai, James A Brunberg, Maureen A Leehey, Lin Zhang, Louise W Gane, Grace Fenton-Farrell, Flora Tassone, Paul J Hagerman.
Abstract
Peripheral neuropathy is common among patients with fragile X-associated tremor ataxia syndrome (FXTAS). Four patients with FXTAS are described with neuropathy as the presenting feature, two having received a prior diagnosis of Charcot-Marie-Tooth (CMT) disease. A fifth is described with neuropathy as the only clinical feature. A functional connection between FXTAS and neuropathy has been suggested by the presence of lamin A/C in the intranuclear, neuronal and astrocytic inclusions of FXTAS, since mutations in lamin A/C are known to give rise to an axonal form of CMT. 2007 Wiley-Liss, IncEntities:
Mesh:
Year: 2007 PMID: 17726686 DOI: 10.1002/ajmg.a.31920
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802