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  Vol. 45 No. 7, July 1988 TABLE OF CONTENTS
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Familial Progressive Vestibulocochlear Dysfunction

Wim I. M. Verhagen, MD; Patrick L. M. Huygen, PhD; Ed M. G. Joosten, MD

Arch Neurol. 1988;45(7):766-768.


Abstract

• A kindred is presented in which several members had complaints of head movement-dependent oscillopsia due to acquired vestibular areflexia in combination with progressive hearing loss. History was noncontributory for other neurologic or otologic diseases (including infectious diseases) or use of neuro-ototoxic drugs. The pedigree suggests autosomal dominant inheritance.



Author Affiliations

From the Department of Neurology, Canisius-Wilhelmina Hospital (Dr Verhagen), and the Institute of Neurology (Drs Verhagen and Joosten) and Department of Otorhinolaryngology (Dr Huygen), Academic Hospital, Nijmegen, the Netherlands.


Footnotes

Accepted for publication Dec 21, 1987.

Reprint requests to Department of Neurology, Canisius-Wilhelmina Hospital, St Annastraat 289, 6525GS, Nijmegen, the Netherlands (Dr Verhagen).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Speech Recognition Scores Related to Age and Degree of Hearing Impairment in DFNA2/KCNQ4 and DFNA9/COCH
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Arch Otolaryngol Head Neck Surg 2001;127:1045-1048.
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A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation
FRANSEN et al.
J. Med. Genet. 2001;38:61-65.
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Familial Progressive Vestibulocochlear Dysfunction Caused by a COCH Mutation (DFNA9)
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Arch Neurol 2000;57:1045-1047.
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Familial Progressive Vestibulocochlear Dysfunction
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Arch Neurol 1991;48:262-262.
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