Objective:

To evaluate the psychological impact of pediatric movement disorders on caregivers and families.

Key Findings:

• Caregivers commonly experience chronic stress, anxiety, depression, and physical health strain.
• Supportive factors such as peer networks, multidisciplinary care, and psychological counseling help mitigate negative effects.
• The influence of sociocultural and religious contexts in the Gulf region affects caregiving experiences and coping patterns.

Interpretation:

The psychological burden experienced by families varies based on the duration, clinical complexity, and type of movement disorder.

Limitations:

• The study is a narrative review and may not encompass all relevant literature.
• Existing validated instruments do not specifically capture the psychological and social dimensions relevant to pediatric movement disorders.

Conclusion:

Future research will focus on systematic validation of the proposed family-centered questionnaire.