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Hearing Acuity and Rh IncompatibilityElectrodermal Thresholds
Noel D. Matkin, PhD;
Raymond Carhart, PhD
Arch Otolaryngol. 1968;87(4):383-388.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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IDENTIFICATION of the site of a lesion responsible for the hearing impairment associated with Rh incompatibility has been attempted through both histologic and audiologic studies. The findings from such investigations are contradictory. On one hand, human tissue studies suggest that icteric pigment deposits have resulted in dysfunction of the central auditory system.1 Such observations have led a number of professional workers to suggest that when a hearing loss occurs as a result of an Rh mismatch it is of the central type. In contrast, two investigators who employed a battery of differential audiological measures with a sample of Rh subjects have obtained profiles of results which are most like those seen in the presence of a cochlear lesion.1,2 However, Carhart3 has suggested that these results are actually the product of damage in the cochlear nuclei which cause behavior that:
... mimic cochlear lesions in many respects and which,
. . . [Full Text PDF of this Article]
Author Affiliations
Evanston, Ill
From the departments of Communicative Disorders and Otolaryngology and Maxillo Surgery, Northwestern University, Evanston, Ill.
Footnotes
Accepted for publication Oct 24, 1967.
Reprint requests to Auditory Research Laboratory, Northwestern University, Evanston, Ill 60201 (Dr. Matkin).
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