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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Congenital sensorineural deafness associated with EEG abnormalities, epilepsy and high familial incidence.

A clinical study was carried out on 31 deaf children attending a school for the deaf in Beer Sheva, Israel. 71 per cent of the pupils were found to have familial deafness. EEG studies showed a high rate of abnormal tracings associated with congenital sensorineural deafness. A significant number of EEGs were paroxysmal. The majority of cases occurred among children with hereditary deafness. Behaviour disturbances were common among the children with abnormal EEGs. One-third of the pupils had additional congenital defects, including three cases of retinitis pigmentosa. Four children (12 X 9 per cent) had epilepsy; two cases of petit mal were of special interest. Hereditary aspects of congenital nerve deafness and the implications of the EEG findings are discussed.[1]

References

  1. Congenital sensorineural deafness associated with EEG abnormalities, epilepsy and high familial incidence. Fishman, J.E., Gadoth, N., Radvan, H. Developmental medicine and child neurology. (1983) [Pubmed]
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