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Short philtrum
URL of this page: //medlineplus.gov/ency/article/003302.htm

Short philtrum

A short philtrum is a shorter than normal distance between the upper lip and the nose.

Considerations

The philtrum is the groove that runs from the top of the lip to the nose.

The length of the philtrum is passed down from parents to their children through genes. This groove is shortened in people with certain conditions.

Causes

This condition can be caused by:

  • Chromosome 18q deletion syndrome
  • Cohen syndrome
  • DiGeorge syndrome
  • Oral-facial-digital syndrome (OFD)

Home Care

No home care is needed for a short philtrum, in most cases. However, if this is only one symptom of another disorder, follow your health care provider's instructions on how to care for the condition.

When to Contact a Medical Professional

Contact your provider if you notice a short philtrum on your child.

What to Expect at Your Office Visit

An infant with a short philtrum may have other symptoms and signs. Taken together, these may define a specific syndrome or condition. The provider will diagnose that condition based on a family history, medical history, and physical exam.

Medical history questions may include:

  • Did you notice this when the child was born?
  • Have any other family members had this feature?
  • Have any other family members been diagnosed with a disorder associated with a short philtrum?
  • What other symptoms are present?

Tests to diagnose a short philtrum:

  • Chromosome studies
  • Enzyme tests
  • Metabolic studies on both mother and infant
  • X-rays

If your provider diagnosed a short philtrum, you may want to note that diagnosis in your personal medical record.

Images

  • The faceThe face
  • PhiltrumPhiltrum

References

Madan-Khetarpal S, Arnold G, Ortiz D. Genetic disorders and dysmorphic conditions. In: Zitelli BJ, McIntire S, Nowalk AJ, Garrison J, eds. Zitelli and Davis' Atlas of Pediatric Physical Diagnosis. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 1.

Sullivan KE, Buckley RH. Primary defects of cellular immunity. 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 151.

Review Date 2/17/2024

Updated by: Charles I. Schwartz, MD, FAAP, Clinical Assistant Professor of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, General Pediatrician at PennCare for Kids, Phoenixville, PA. 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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