3341-3350 of 3455 Results Found
Condition
Obstructive Sleep Apnea in Children What is obstructive sleep apnea in children? Obstructive sleep apnea is when a child briefly stops breathing while sleeping. It happens because of a blockage in the upper airway. This is the passages through the nose and mouth to the windpipe
Condition
Tetralogy of Fallot (TOF) What is tetralogy of Fallot? Tetralogy of Fallot (TOF) is a set of 4 congenital heart defects that happen together. Tetralogy refers to the number 4. Congenital means that a baby is born with them. The set of 4 defects are: Narrowing (stenosis) of the
Condition
Congenital Laryngeal Stridor in Babies What is congenital laryngeal stridor? Congenital laryngeal stridor is a noisy or high-pitched sound with breathing. It is from an abnormally formed voice box (larynx). It's present at birth (congenital). What causes congenital laryngeal
Condition
Dermoid Cyst in Children What are dermoid cysts in children? A dermoid cyst is a collection of tissue under the skin. It may contain hair follicles, oil, and sweat glands. In some cases, it may contain bone, teeth, or nerves. A dermoid cyst may appear at birth or soon after
Condition
Transposition of the Great Arteries (TGA) in Children What is transposition of the great arteries in children? Transposition of the great arteries (TGA) is a type of heart defect that your baby is born with (congenital). In this condition, the two arteries that carry blood out of
Condition
Truncus Arteriosus (TA) What is truncus arteriosus? Truncus arteriosus is a heart defect that is present at birth (congenital). It happens when there is an abnormal connection between the aorta and pulmonary artery. Normally, the aorta and the pulmonary artery are separate. In
Condition
Types of Hearing Loss in Children What are the different types of hearing loss? There are 3 main types of hearing loss: sensorineural, conductive, and mixed (both sensorineural and conductive). These types of hearing loss can be present at birth (congenital). Or they can happen
Condition
22q11.2 Deletion Syndrome in Children What is 22q11.2 deletion syndrome in children? The 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder. In children with this syndrome, a tiny piece of chromosome 22 is missing. This can cause many health problems. These problems may
Condition
Overview of Craniofacial Anomalies What are craniofacial anomalies? Craniofacial anomalies (CFA) are a variety of deformities in the growth of the head and facial bones. Anomaly is a medical term meaning different from normal. These abnormalities are present at birth (congenital)
Condition
The Craniofacial Team When should my child see a craniofacial team? The best time for the first assessment of craniofacial abnormalities is within your child's first few weeks of life. The focus of the team visit is to help correct your child's medical problems and to ease