A BS TRACT: PD is a progressive and complex neurological disorder with heterogeneous symptomatology. PD is characterized by classical motor features of parkinsonism and nonmotor symptoms and involves extensive regions of the nervous system, various neurotransmitters, and protein aggregates. Extensive evidence supports auditory dysfunction as an additional nonmotor feature of PD. Studies indicate a broad range of auditory impairments in PD, from the peripheral hearing system to the auditory brainstem and cortical areas. For instance, research demonstrates a higher occurrence of hearing loss in early-onset PD and evidence of abnormal auditory evoked potentials, event-related potentials, and habituation to novel stimuli. Electrophysiological data, such as auditory P3a, also is suggested as a sensitive measure of illness duration and severity. Improvement in auditory responses following dopaminergic therapies also indicates the presence of similar neurotransmitters (i.e., glutamate and dopamine) in the auditory system and basal ganglia. Nonetheless, hearing impairments in PD have received little attention in clinical practice so far. This review summarizes evidence of peripheral and central auditory impairments in PD and provides conclusions and directions for future empirical and clinical research.Among neurological disorders, which are the leading cause of disability in the world, Parkinson's disease (PD) shows the highest growth in prevalence, rate of deaths, and disability-adjusted life-years between 1990 and 2015, and it is estimated to double over the next 20 years. 1 The etiology of PD is often unknown and mostly occurs in sporadic form, possibly arising from the association of genetic and environmental risk factors. 2,3 As a progressive disease, PD is characterized by early major death of dopaminergic neurons in the SNpc within the basal ganglia that leads to classical parkinsonian and secondary motor symptoms. 2,4 PD pathology involves extensive regions of the nervous system, various neurotransmitters (e.g., dopaminergic and nondopaminergic neurotransmitters), and protein aggregations other than just Lewy bodies or Lewy neurites (i.e., abnormal aggregation of insoluble α-synuclein protein [SNCA]) 2 that account for a wide range of clinical symptoms and signs observed in PD. 5 Thus, multiple nonmotor symptoms (NMSs) develop throughout the PD progress, some of which precede the motor dysfunction by more than a decade. 2 For instance, fatigue, neuropsychiatric symptoms, autonomic dysfunction, gastrointestinal symptoms, sensory deficits (e.g., visual impairments, 6 olfactory dysfunction, 7 taste disorders, 8 somatosensory abnormalities, 9 and auditory disorders 10,11 ), and sleep problems are within common NMSs in early PD. 2,3 Among sensory dysfunctions as NMSs of PD, somatic sensations, such as pain and paraesthesias, have received ---