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question 9 (mandatory) (10 points) listen the disease/condition that is inherited with an autosomal dominant mode of inheritance and that manifests with bilateral acoustic neuromas, progressive loss of motor function, deafness, paralysis, and eventual death? neurofibromatosis type ii neurofibromatosis type 1 von recklinghausens disease amyotrophic lateral sclerosis
Neurofibromatosis type II is an autosomal - dominant disorder characterized by bilateral acoustic neuromas and can lead to progressive motor function loss, deafness, paralysis, and death. Neurofibromatosis type 1 and Von Recklinghausen's disease (which is another name for type 1) mainly present with skin and nerve - related symptoms other than the specific bilateral acoustic neuromas as described. Amyotrophic Lateral Sclerosis is a neurodegenerative disease not characterized by bilateral acoustic neuromas and has a different genetic and clinical profile.
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Neurofibromatosis type II