Parietal Foramina
Abnormal, symmetric, oval openings in the PARIETAL BONE on each side of the sagittal suture and separated from each other by a narrow bridge of bone. Their size decreases with age and considerable intrafamilial variability is observed. Mutations in the MSX2 and ALX4 genes have been identified for some cases. OMIM: 168500.
Also Known As:
Catlin Marks; Cranium Bifidum Occultum; Cranium Bifidum, Hereditary; Enlarged Parietal Foramina; Foramina Parietalia Permagna; Parietal Foramina, Symmetric
Networked: 13
relevant articles (0 outcomes,
1 trials/studies)
Disease Context: Research Results
Related Diseases
Experts
1. | Galvão, André Pukey Oliveira:
1 article
(07/2021)
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2. | Magalhães, Carolina Peixoto:
1 article
(07/2021)
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3. | Valença, Marcelo Moraes:
1 article
(07/2021)
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4. | de Queiroz Lima, Alessandra Mertens Brainer:
1 article
(07/2021)
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5. | de Queiroz Lima, Pedro Thadeu Mertens Brainer:
1 article
(07/2021)
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6. | de Souza Ferreira, Maria Rosana:
1 article
(07/2021)
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7. | Da Costa Val Filho, José Aloysio:
1 article
(05/2021)
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8. | Dantas Dos Santos, Aieska Kellen:
1 article
(05/2021)
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9. | Ferreira Furtado, Leopoldo Mandic:
1 article
(05/2021)
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10. | Lima Vieira, José Antônio:
1 article
(05/2021)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Parietal Foramina:
Therapies and Procedures