Literature DB >> 223494

Abnormal auditory evoked potentials in hereditary motor-sensory neuropathy.

S Satya-Murti, A T Cacace, P A Hanson.   

Abstract

From a kinship with a dominantly inherited motor-sensory neuropathy, we studied 2 brothers with brainstem auditory evoked potentials and behavioral audiometric tests. They had abnormal prolongation of I-III interpeak intervals. Wave V was poorly developed. Conventional audiometric tests did not reveal a peripheral hearing loss. It is probable that their auditory nerves and spiral ganglia are undergoing a pathophysiological process analogous to that of their peripheral nerves.

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Year:  1979        PMID: 223494     DOI: 10.1002/ana.410050506

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  7 in total

1.  Abnormal auditory evoked potentials in Déjérine-Sottas disease. Report of two cases with central acoustic and vestibular impairment.

Authors:  F Baiocco; D Testa; A d'Angelo; F Cocchini
Journal:  J Neurol       Date:  1984       Impact factor: 4.849

2.  Peripheral and central conduction times in hereditary pressure-sensitive neuropathy.

Authors:  A Ebner; R Dengler; C Meier
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

3.  Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses.

Authors:  G Nicholson; A Corbett
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-07       Impact factor: 10.154

4.  Auditory brain-stem responses in the fragile X syndrome.

Authors:  T Arinami; M Sato; S Nakajima; I Kondo
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

5.  F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.

Authors:  V Scaioli; D Pareyson; G Avanzini; A Sghirlanzoni
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-11       Impact factor: 10.154

6.  Trigeminal and facial nerve involvement in Charcot-Marie-Tooth disease. An electrodiagnostic study.

Authors:  J P Malin
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

7.  Peroneal muscular atrophy with ataxia and partial myoclonic epilepsy.

Authors:  C Angelini; G F Micaglio; M Armani; S Pierobon-Bormioli; R Giordano; G F Testa
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

  7 in total

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