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Table 10 Comparison based on working experience (Domain 1)

From: Knowledge of genetics of hearing and genetic counseling among practicing audiologists

Non-syndromic hearing loss

Correct

response N (%)

Incorrect

response N (%)

(1) What percentage of the hearing losses are non-syndromic?

  Less than 5 years

51 (68.92%)

23 (31.08%)

  5 or more than 5 years

12 (20.3%)

47 (79.6%)

(2) In autosomal recessive inheritance, how many copies of an abnormal gene must be present for the trait to develop?

  Less than 5 years

62 (83.78%)

12 (16.22%)

  5 or more than 5 years

43 (72.8%)

16 (27.12%)

(3) Select the most common gene mutation causing non-syndromic hearing loss

  Less than 5 years

39 (52.7%)

35 (47.3%)

  5 or more than 5 years

51 (86.44%)

8 (13.56%)

(4) Sporadic mutation can occur in children with?

  Less than 5 years

49 (66.22%)

25 (33.78%)

  5 or more than 5 years

35 (59.32%)

24 (40.68%)

(5) Mutation in which gene causes auditory neuropathy?

  Less than 5 years

45 (60.81%)

29 (39.19%)

  5 or more than 5 years

42 (71.19%)

17 (28.81%)

(6) The age of onset of non-syndromic hearing loss can be?

  Less than 5 years

62 (83.78%)

12 (16.22%)

  5 or more than 5 years

49 (83.05%)

10 (16.95%)

(7) DFNA9 gene mutation causes?

  Less than 5 years

48 (64.86%)

26 (35.14%)

  5 or more than 5 years

41 (69.49%)

18 (30.51%)

  1. P value- 0.712, > 0.05