A possible role of dystrophin in neuronal excitability: A review of the current literature

作者：Hendriksen Ruben G F^*; Hoogland Govert; Schipper Sandra; Hendriksen Jos G M; Vles Johan S H; Aalbers Marlien W

来源：Neuroscience and Biobehavioral Reviews, 2015, 51: 255-262.

DOI：10.1016/j.neubiorev.2015.01.023

• Duchenne muscular dystrophy
• Dystrophin
• Epilepsy
• Seizures

Duchenne muscular dystrophy (DMD) is a recessive hereditary form of muscular dystrophy caused by a mutation in the dystrophin gene on the X chromosome. Clinical observations show that in addition to progressive muscular degeneration, DMD is more often accompanied by neurocognitive symptoms and learning disabilities, especially in automatisation of reading, attention processes, and expressive language skills. Additionally, three studies reported a higher prevalence of epilepsy in DMD, suggesting that the absence of dystrophin might be related to increased CNS excitability. In this article, we aim to review current clinical and experimental evidence for a potential role of brain dystrophin in seizure generation.

• 出版日期2015-4