Detailed anatomical information on the newborn skull.

Detailed information on craniofacial anomalies, including Cleft Lip, Cleft Palate, Craniosynostosis, Deformational Plagiocephaly, Hemifacial Microsomia, Vascular Malformations, and Hemangiomas

Detailed information on craniofacial anomalies, including Cleft Lip, Cleft Palate, Craniosynostosis, Deformational Plagiocephaly, Hemifacial Microsomia, Vascular Malformations, and Hemangiomas

Hemifacial microsomia (HFM) is a congenital disorder. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped (hemi means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.

Read this for information about a first assessment of any craniofacial abnormalities your child may have and the craniofacial treatment team that will treat them.

Detailed information on craniofacial anomalies, including cleft lip, cleft palate, craniosynostosis, hemifacial microsomia, vascular malformation, hemangioma, and deformational plagiocephaly.

22q11.2 deletion syndrome is a genetic disorder that can cause many health problems. These problems may range from heart defects and developmental delays to seizures.

An ultrafast computed tomography (CT) scan is an imaging test that uses X-rays and a computer to look at your child’s heart. It gives the doctor many details about your child’s heart that other imaging tests can’t. Learn more about what you can expect when your child has this test.

Common variable immunodeficiency (CVID) is an immunodeficiency problem. It is a lifelong health problem that can lead to a reduced ability to fight infections.

The tilt table test is done to find the cause of fainting (syncope). Tilt table testing is done with a special table or bed that changes a child's position from lying to standing. Their blood pressure and heart rate are checked while they're in the different positions.