Genetic study of deafness in Pakistani families
Part of Brain & nervous system, Ear, nose & throat, Eyes & vision, Genetic & congenital clinical trials.
This study looks at genetic causes of deafness by comparing affected and unaffected family members. It may help researchers understand why some people are born or develop deafness and guide future diagnosis for families in Pakistan.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a family with members who are deaf and members who are not
- Your deafness is believed to be genetic (not from infection, injury, loud noise, or medicine that can harm hearing)
- If you are an adult, you can give informed consent (agree to join after being told the study)
- If you are a parent/guardian, you (or your child’s parent/guardian) can give informed consent
- If your child is being included, they must be at least 2 years old
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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