Question

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 1 von recklinghausens disease neurofibromatosis type ii amyotrophic lateral sclerosis

Explanation:

Neurofibromatosis type II is an autosomal - dominant disorder characterized by bilateral acoustic neuromas, which can lead to progressive loss of motor function, deafness, paralysis, and eventually death. Neurofibromatosis type 1 (also known as Von Recklinghausen's disease) has different manifestations mainly involving skin and peripheral nerve tumors. Amyotrophic Lateral Sclerosis is not characterized by bilateral acoustic neuromas.

Answer:

C. Neurofibromatosis type II