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Metopic ridge
URL of this page: //medlineplus.gov/ency/article/003312.htm

Metopic ridge

A metopic ridge is an abnormal shape of the skull. The ridge can be seen on the forehead.

Considerations

The skull of an infant is made up of bony plates. The gaps between the plates allow for growth of the skull. The places where these plates connect are called sutures or suture lines. They do not fully close until the 2nd or 3rd year of life.

A metopic ridge occurs when the 2 bony plates in the front part of the skull join together too early.

The metopic suture remains unclosed throughout life in 1 in 10 people.

Causes

A birth defect called craniosynostosis is a common cause of metopic ridge. It can also be associated with other congenital skeletal defects.

When to Contact a Medical Professional

Contact your health care provider if you notice a ridge along your infant's forehead or a ridge forming on the skull.

The provider will perform a physical exam and ask questions about the child's medical history.

Tests may include:

  • Head CT scan
  • Skull x-ray

A metopic ridge must be differentiated from metopic synostosis, which is a more serious condition. Parents can find information and support at www.cappskids.org/metopic-ridge/.

No treatment or surgery is needed for a metopic ridge if it is the only skull abnormality.

Images

  • Metopic ridgeMetopic ridge
  • The faceThe face

References

Craniosynostosis and Positional Plagiocephaly Support (CAPPS) website. The metopic ridge/benign or surgical? www.cappskids.org/metopic-ridge/. Accessed December 5, 2023.

Graham JM, Sanchez-Lara PA. Craniosynostosis: general. In: Graham JM, Sanchez-Lara PA, eds. Smith's Recognizable Patterns of Human Deformation. 5th ed. Philadelphia, PA: Elsevier; 2025:chap 29.

Jha RT, Magge SN, Keating RF. Diagnosis and surgical options for craniosynostosis. In: Ellenbogen RG, Sekhar LN, Kitchen ND, da Silva HB, eds. Principles of Neurological Surgery. 4th ed. Philadelphia, PA: Elsevier; 2018:chap 9.

Kinsman SL, Johnston MV. Congenital anomalies of the central nervous system. In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics. 21st ed. Philadelphia, PA: Elsevier; 2020:chap 609.

Qi R, Piggott K, Lloyd-White S, Kearney A. Developmental outcomes for children with unoperated metopic or sagittal craniosynostosis: Findings at 3 and 7 years from the craniofacial collaboration UK. J Craniofac Surg. 2023;34(7):1953-1958. PMID: 37264505 pubmed.ncbi.nlm.nih.gov/37264505/.

Shakir S, Taylor JA. Nonsyndromic craniosynostosis. In: Losee JE, Hopper RA, eds. Plastic Surgery: Volume 3: Craniofacial, Head and Neck Surgery and Pediatric Plastic Surgery. 5th ed. Philadelphia, PA: Elsevier; 2024:chap 25.2.

Review Date 11/8/2023

Updated by: Franklin W. Lusby, MD, Ophthalmologist, Lusby Vision Institute, La Jolla, CA. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

Related MedlinePlus Health Topics

  • Craniofacial Abnormalities

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The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only – they do not constitute endorsements of those other sites. No warranty of any kind, either expressed or implied, is made as to the accuracy, reliability, timeliness, or correctness of any translations made by a third-party service of the information provided herein into any other language. © 1997-2025 A.D.A.M., a business unit of Ebix, Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

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