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Table 6 Comparison of knowledge between both groups of graduates (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? (50%)

  

 M.ASLP

52 (75.36%)

17 (24.64%)

 M.Sc. Audiology

16 (25%)

48 (75%)

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

  

 M.ASLP

54 (78.26%)

15 (21.74%)

 M.Sc. Audiology

39 (60.94%)

25 (39.06%)

(3) Select the most common gene mutation causing non-syndromic hearing loss. (GJB2)

  

 M.ASLP

60 (86.96%)

9 (13.04%)

 M.Sc. Audiology

53 (82.81%)

11 (17.19%)

(4) Sporadic mutation can occur in children with? (Healthy parents)

  

 M.ASLP

29 (42.03%)

40 (57.97%)

 M.Sc. Audiology

45 (70.31%)

19 (29.69%)

(5) Mutation in which gene causes auditory neuropathy? (OTOF)

  

 M.ASLP

45 (65.22%)

24 (34.78%)

 M.Sc. Audiology

45 (70.31%)

19 (29.69%)

(7) The age of onset of non-syndromic hearing loss can be? (Both—pre-lingual and post-lingual)

  

 M.ASLP

55 (79.71%)

14 (20.29%)

 M.Sc. Audiology

56 (87.5%)

8 (12.5%)

(8) DFNA9 gene mutation causes? (Late-onset progressive sensorineural hearing loss

  

 M.ASLP

44 (63.77%)

25 (36.23%)

 M.Sc. Audiology

45 (70.31%)

19 (29.69%)

  1. (P value = .361, > .05)