| Literature DB >> 30006721 |
Marianthi Breza1, Georgios Koutsis2.
Abstract
Spinal and bulbar muscular atrophy (SBMA), also known as Kennedy's disease, is a rare, X-linked hereditary lower motor neuron disease, characterized by progressive muscular weakness. An expanded trinucleotide repeat (CAG > 37) in the androgen receptor gene (AR), encoding glutamine, is the mutation responsible for Kennedy's disease. Toxicity of this mutant protein affects both motor neurons and muscles. In this review, we provide a comprehensive, clinically oriented overview of the current literature regarding Kennedy's disease, highlighting gaps in our knowledge that remain to be addressed in further research. Kennedy's disease mimics are also discussed, as are ongoing and recently completed therapeutic endeavours.Entities:
Keywords: Androgen receptor; Kennedy’s disease; Spinal and bulbar muscular atrophy; Spinobulbar muscular atrophy; X-linked
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Year: 2018 PMID: 30006721 DOI: 10.1007/s00415-018-8968-7
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849