Ear Deformities

Types of Ear Deformities

Ear deformities are one of the most common birth defects, experienced by roughly 45% of newborns. Despite their frequency, ear deformities are often overlooked by parents and hospital staff.

Fortunately, there are many treatment options available that can correct these common ear deformities. In many cases, the earlier corrective medical treatment is done, the better.

With today’s technology and improved knowledge of ear deformities, corrective treatment can be done on newborns shortly after birth.

Below are some of the most common ear deformities. Some ear deformities improve, and may even go away over time by their own, some may require medical treatment in the form of corrective surgery and some ear deformities can’t be properly treated.

Helical Rim

The Helical Rim is the folded “C” shaped part of the outer ear. Sometimes this part of the ear can become irregularly shaped or compressed.

Stahl’s Ear

The Stahl’s ear deformity, which is sometimes called Elf Ear or Spock Ear, is where the transverse crus doesn’t gently ben upward towards the triangular fossa, but rather it extends outward from the antihelix.

This type of ear deformity is often present in addition to other physical deformities.

Cup Ear

Cup ear is a form of prominent ear that also features an incomplete ear opening. In addition, the cartilage of the Helical Rim and the scapha is stiff and inflexible.


With lidding, the upper third of the ear or the Helical Rim is folded over.  The cause of lidding is the improper formation and development of either the fossa or the antihelix parts of the ear. The most extreme case of lidding results in lop ear.

Conchal Crus

Conchal Crus is when there is an abnormality in the folding of the cartilage of the concha symba. This deformity gives the ear the appearance that it is cut in half. This unusual division of the ear can extend all the way to the back wall of the ear. This condition cuts off the conchal hollow. Conchal Crus can lead to prominent ear, a condition where the ear protrudes out from the side of the head.

Prominent Ear

Those with prominent ear have one or two ears that protrude further than the normal 9mm from the head. This condition is often undiagnosed or under-diagnosed in infants as there are no hearing loss or difficulties associated with it. In some cases, the abnormal protrusion of the ear isn’t noticed by parents until the child is older. Early treatment is important to fully correct this issue.


Those with Cryptotia have an ear where the upper portion of the ear is buried underneath the side of the head. Because of this, the condition is also sometimes called hidden ear or buried ear.  With Cryptotia, the antihelical crura and the scapha are under-developed.

Treating Ear Deformities

Children with minor ear deformities that don’t affect their hearing may not need treatment. Those who have more severe ear deformities that affect their ability to hear and which may contribute to other physical or mental health conditions will most likely require medical treatment.

Restoring a child’s hearing ability and correcting the shape of ear are common purposes of ear surgery. The most effective treatment is based on the specific ear deformity, the age of the patient and the severity of the ear deformity. The ear molding procedure, for instance, can be done within the first week of a baby’s life and is effective in treating Stahl’s ears, constricted and protruding ears. Ear reconstruction surgery is often recommended when children are at least 6 years of age. Below are common medical treatment options for correcting children’s ear deformities:

  • Ear Splints
  • Ear Molding
  • Surgery
  • Hearing Aids and Cochlear Implants
  • Infant Ear Correction System

At Cleft & Craniofacial Institute of Utah, we offer newborns with ear deformities a non-surgical, non-invasive ear correction system called EarWell. This treatment can be started within days of a baby’s birth and requires no sedation, medication or anesthesia. It is pain-free and highly effective.

However, for the best chance of full correction, the EarWell treatment must begin when the child is no more than three months old.

The ability to hear and feel comfortable in one’s own skin are important at the Cleft & Craniofacial Institute of Utah, we diagnose and treat each patient individually so they can have the best quality of life as possible.

Consult with Dr. Griner

If you suspect that your baby may have an ear deformity, contact the Cleft & Craniofacial Institute of Utah to schedule a consultation to learn more about the various treatment options for your child’s ear deformity.

Our Expertise

Cleft Lip/Palate

 Cleft lips and palates are one of the most common birth anomalies that affect about 1/600 newborn babies in the United States and around 1/500 in the state of Utah.  Clefts can range from quite mild to fairly severe.  Most of the time they are an isolated anomaly, but are also associated with a number of gentic syndromes.  Depending on what structures are involved dictates the complexity of the treatment plan.   Our team works together with you to make a customized plan for  your baby.  Even the most severe of cases should be able to be treated with only a few surgical interventions by a well coordinated and efficient team.






The skull is made up of several different bones that are joined together by growth plates called "sutures."  Craniosynostosis is a condition where one or more of these sutures fuse prematurely causing an abnormal head shape, decreased cranial volume, and the possiblilty of raised intracranial pressure.  The treatment of craniosynostosis is surgical and the goals of surgery are to increase the volume of the skul and to correct the abnormal appearance of the head shape.  There are two methods of surgical correction: open vault reconstruction and strip craniectomy.  Dr. Griner's extensive training allows him to perform these complex procedures without the need for blood transfusions and spending only 1-2 nights in the hospital. 



There are many syndromes that can affect the shape of the head and face and include Aperts, Crouzon, Pfieffer, Treacher Collins, and many others.  Most of these syndromes include many other complex anomalies and need to be treated in a coordinated approach in order to reduce the number of operations the child will need.  These syndromes are rare and require specialists that are very familiar with the intricacies of each syndrome.  Dr. Griner's unique training provided him with extensive experience with craniofacial syndromes and makes him the premier choice to guide the management of your child's needs in Utah.





Ear Deformities

Ear deformities range from mild changes in shape to the complete abscence of an ear and deafness.  Mild deformities can be treated in the first few weeks of life while others will require reconstructive surgery and hearing aids.  No matter the severity, our specialists work together to provide normal appearance and improved hearing.


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