Related Experiment Videos
Hearing disorders in sickle cell disease: cochlear and retrocochlear findings
H J Gould1, M R Crawford, W R Smith
1Memphis State University, Tennessee.
Ear and Hearing
|October 1, 1991
Summary
Adults with sickle cell disease face risks of auditory system dysfunction. Regular hearing tests are crucial for monitoring cochlear and retro-cochlear health in these patients.
Area of Science:
- Otorhinolaryngology
- Hematology
- Audiology
Background:
- Sickle cell disease (SCD) is a genetic blood disorder with potential systemic complications.
- Auditory system involvement in SCD is not fully understood, necessitating further investigation.
Purpose of the Study:
- To assess the auditory system in adult patients with sickle cell disease.
- To identify potential auditory dysfunctions associated with SCD.
Main Methods:
- Standard audiometric test techniques were employed.
- The study included 34 adult subjects diagnosed with sickle cell disease.
Main Results:
- Patients with SCD are susceptible to both cochlear and retro-cochlear auditory dysfunction.
- No specific audiometric pattern uniquely identifies sickle cell disease.
Conclusions:
- Auditory status requires careful and consistent monitoring in all adult SCD patients.
- Early detection of auditory issues can aid in managing SCD-related complications.