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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

1. Craniosynostoses (Craniosynostosis)
2. Synostosis
3. Hypertelorism
4. Congenital Abnormalities (Deformity)

Experts

1. Galvão, André Pukey Oliveira: 1 article (07/2021)
2. Magalhães, Carolina Peixoto: 1 article (07/2021)
3. Valença, Marcelo Moraes: 1 article (07/2021)
4. de Queiroz Lima, Alessandra Mertens Brainer: 1 article (07/2021)
5. de Queiroz Lima, Pedro Thadeu Mertens Brainer: 1 article (07/2021)
6. de Souza Ferreira, Maria Rosana: 1 article (07/2021)
7. Da Costa Val Filho, José Aloysio: 1 article (05/2021)
8. Dantas Dos Santos, Aieska Kellen: 1 article (05/2021)
9. Ferreira Furtado, Leopoldo Mandic: 1 article (05/2021)
10. Lima Vieira, José Antônio: 1 article (05/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Parietal Foramina:
1. DNA (Deoxyribonucleic Acid)IBA
2. Polyethylene (Polythene)IBA
3. 4- Acetamido- 4'- isothiocyanatostilbene- 2,2'- disulfonic Acid (SITS)IBA
4. LigandsIBA

Therapies and Procedures

1. Sutures (Suture)
2. Piezosurgery
3. Osteotomy
4. Craniotomy