Table 3.
Type of consultation | Number (n = 126) | Percentage |
---|---|---|
The risk assessment for autosomal recessive diseases | 95 | 75 % |
The risk screening for disease X-linked | 71 | 56 % |
The risk assessment for autosomal dominant diseases | 81 | 64 % |
Presymptomatic or predictive (non-cancerous) testing of autosomal dominant diseases | 27 | 21 % |
Presymptomatic testing for familial cancer | 42 | 33 % |
Genetic counselling for consanguinity | 83 | 66 % |
Consultations for medically assisted procreation | 67 | 53 % |
Consultations for prenatal diagnosis | 67 | 53 % |