Table VI.
Suggestions for Targeted Psychosocial History/Assessment
| Level of education |
| Possible barriers to communication, including cultural/language diversity or the presence of learning disabilities |
| Current level of knowledge regarding diagnosis of NF1 |
| Family’s understanding and perception of medical information |
| Previous experiences with NF1, if any |
| Family’s perception of the etiology of NF1 |
| Emotional reaction to the diagnosis of NF1 |
| Family structure and functioning |
| Family and community support systems |
| Coping skills |
| Meaning of a genetic diagnosis for the family, including implications for family planning and parenting |