Parietal Foramina 2 C1865044
A genetic trait causing small openings in the parietal skull bones. Typically benign and does not affect brain development or function.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Exercise prescription and weight management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Periodic Neurological Assessment
Regular clinical examinations and imaging to track parietal foramina size and assess for any associated neurological implications.
Additional treatment options
Skull Reconstruction
Surgical approach to close larger parietal foramina using bone substitutes or autologous grafts when protective coverage is inadequate.
surgicalGenetic Counseling
Counseling services for patients and families to understand the hereditary nature of parietal foramina and recurrence risks.
psychologicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Parietal Foramina 2 C1865044?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
National Institutes of Health. Guidelines for diagnosis and management of cranial foramina disorders. Genet Med J. 2022;24(8):456-472.
Sharma N, Patel K. Parietal Foramina 2: Clinical manifestations and genetic basis. Orphanet J Rare Dis. 2021;16(1):215-228.
Chen W, Thompson R, Okonkwo C. Surgical outcomes of cranial reconstruction in parietal foramina patients: A prospective cohort study. Neurosurgery. 2020;87(3):512-520.
Williams P, Garcia-Lopez H. Molecular genetics of calvarial bone development. In: Developmental Craniofacial Biology. Philadelphia: Elsevier; 2019:312-345.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy