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Parietal Foramina
An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, is caused by mutation in the ALX4 gene or MSX2 gene.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, is caused by mutation in the ALX4 gene or MSX2 gene.
Resources
Join the Parietal Foramina community
Talk with people who understand, share what helps, and find support from others living with parietal foramina. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.