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Name
  Reason for Consult
Email
  Phone
Comment
Joel in 2007. Condition: Unilateral Cleft Lip and Palate

Joel in 2007

Current Age:
4 years old

Condition:
Unilateral Cleft Lip and Palate

Joel - 4 years old
Jackson in 2007. Condition: Bilateral Cleft Lip and Palate

Jackson in 2007

Current Age:
11 years old

Condition:
Microtia and Hemifacial Microsomia

Jackson - 11 years old
Jessie in 2006. Condition: Bilateral Cleft Lip and Palate

Jessie in 2006

Current Age:
5 years old

Condition:
Bilateral Cleft Lip and Palate

Jessie - 5 years old
Trevor in 2006. Condition: Sagittal Synostosis.

Trevor in 2006

Current Age:
4 years old

Condition:
Sagittal Synostosis

Trevor - 4 years old
Stella in 2006. Condition: Bilateral Cleft Lip and Palate

Stella in 2009

Current Age:
11 months old

Condition:
Bilateral Cleft Lip and Palate

Stella - 11 month old
Forest Park Medical Center

Common Conditions and Syndromes

One in every 700 births results in a cleft lip and/or palate – many within families that have no history of clefts. While it is known how clefts occur, it is seldom known why. Most importantly, clefts are correctable, and ICI is here to make that happen.

The malformation of either one or both ears, microtia can occur by itself or as part of hemifacial microsomia, Goldenhar syndrome or Treacher Collins syndrome. At ICI, we can help with any and all forms of microtia, as well as assessing and managing any associated hearing loss.

Craniosynostosis is a congenital defect that causes one or more sutures on a baby's head to close earlier than normal, resulting in an abnormally shaped head. At ICI, we are adamant about educating our families about all the forms of craniosynostosis in order to address the condition appropriately right from the start.

We specialize in a variety of craniofacial conditions. Our highly skilled team is experienced in repairing and correcting even the most difficult, rare, inherited and/or acquired head, face, neck and jaw anomalies.

Your family is Our family.

Our goal is for every
patient to leave smiling.
Whether you or your child
has inherited or acquired a
craniofacial anomaly, we are
dedicated to finding the best
possible solution to fit your needs.
No matter how difficult or how rare
your craniofacial disorder, we will
do everything we can to help. Because at
the International Craniofacial Institute, your
family is our family.

Visit our Family Forum

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