| Literature DB >> 16193596 |
Kimitaka Kaga1, Fumi Tamai, Mariko Kodama, Kazuo Kodama.
Abstract
Three young adult males with Pelizaeus-Merzbacher disease have been followed up since childhood. This disease is thought to be a dysmyelinating disorder of the brain during the prenatal period caused by gene mutations. The patients manifested horizontal nystagmus and severe rigidity of the extremities. Although the patients showed only waves I and II in auditory brainstem responses, they had relatively good hearing ability at approximately equal to dB. They could not speak words at all but could hear well and enjoy listening to conversation and music. One of them had a normal hearing threshold in pure-tone audiometry and a normal speech discrimination rate in speech audiometry. This can be explained by a nerve conduction blockade through dysmyelinated axons or the desynchronization of neurons and nerves responsible for the waves following waves I and II. At present, all three patients are living with their families. We report their present hearing, speech and language abilities.Entities:
Mesh:
Year: 2005 PMID: 16193596 DOI: 10.1080/00016480510038581
Source DB: PubMed Journal: Acta Otolaryngol ISSN: 0001-6489 Impact factor: 1.494