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.

Detailed information on craniofacial abnormalities and the craniofacial treatment team.

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 healthcare provider many details about your child’s heart that other imaging tests can’t.

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.

Contact dermatitis is a skin reaction from contact with certain substances. Read on to learn about its causes, symptoms, and treatment.

Detailed information on heart defects that cause too little blood flow through the lungs

Atopic dermatitis is a long-term (chronic) skin condition. It causes dry, itchy skin. It’s very common in babies and children. It often first appears between ages 3 and 6 months.