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Disease: Vestibulocochlear dysfunction progressive familial

  • AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance
  • Dominant hereditary nerve deafness
  • Early and late damage to the auditory and vestibular area after meningitis in childhood and adolescence
  • Eighth cranial nerve dysfunction in hyperostosis cranialis interna
  • Familial progressive vestibulocochlear dysfunction
  • Familial progressive vestibulocochlear dysfunction
  • Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)
  • Hereditary vestibulo-cochlear dysfunction and vascular disorders
  • Neuro-otological manifestations in Fabry disease-a retrospective single center study
  • Neurophysiologic, audiometric and vestibular function tests in patients with hyperostosis cranialis interna
  • Phenotypic manifestations and management of hyperostosis cranialis interna, a hereditary bone dysplasia affecting the calvaria and the skull base
  • Progressive cranial nerve involvement and grading of facial paralysis in gelsolin amyloidosis
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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