Metopism

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Metopism
Synonyms	Persistent metopic suture
Pronounce	N/A
Specialty	N/A
Symptoms	Presence of a suture line on the frontal bone
Complications	None
Onset	Birth
Duration	Lifelong
Types	N/A
Causes	Genetic factors, developmental variation
Risks	None
Diagnosis	Radiography, CT scan
Differential diagnosis	Craniosynostosis
Prevention	N/A
Treatment	None required
Medication	N/A
Prognosis	Excellent
Frequency	Varies by population
Deaths	N/A

Fontanelle

Metopism refers to the persistence of the metopic suture, also known as the frontal suture, in the forehead beyond early childhood. Normally, this suture, which runs down the midline of the skull from the top of the head down the forehead to the nose, fuses between the ages of 3 to 9 years. When this suture does not fuse and remains visible in adulthood, the condition is termed metopism.

Introduction

The human skull is made up of several plates of bone that are separated by sutures at birth. These sutures allow for growth of the skull and the brain during infancy and childhood. One of these, the metopic suture, divides the frontal bone into two halves. In most individuals, this suture closes in early childhood, but in some cases, it remains open or partially open, a condition known as metopism.

Epidemiology

Metopism is relatively rare, with its prevalence varying among different populations. It is more commonly observed in males than in females. The exact reasons for the variation in the rate of closure of the metopic suture are not fully understood but are thought to involve genetic and environmental factors.

Clinical Significance

In most cases, metopism is simply a normal anatomical variant with no clinical significance. However, in some instances, it can be associated with certain craniofacial syndromes or abnormalities. Therefore, if metopism is observed, especially if it is pronounced or accompanied by other cranial anomalies, further evaluation may be warranted to rule out underlying conditions.

Diagnosis

Diagnosis of metopism is primarily based on physical examination and imaging studies such as X-rays or CT scans. These imaging techniques can help to visualize the extent of suture patency and identify any associated cranial abnormalities.

Treatment

For the majority of individuals with metopism, no treatment is necessary. In cases where metopism is associated with craniofacial syndromes or other abnormalities, treatment may be directed towards the underlying condition.

Summary

Metopism is a rare condition characterized by the non-fusion of the metopic suture. While it is usually of no clinical significance, its presence can sometimes indicate underlying cranial abnormalities. As such, individuals with pronounced metopism should undergo further evaluation to ensure there are no associated conditions.

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