22q11.2 deletion syndrome is a genetic condition that causes a combination of medical problems. These problems may include heart defects, cleft palate, speech or feeding problems, difficulty fighting infections, low...
Acute disseminated encephalomyelitis (ADEM) involves a brief but intense attack of inflammation (swelling) in the brain and spinal cord that damages the brain's myelin.
Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental issue where people have trouble paying attention and controlling impulses.
Developmental delays refer to when developmental skills are at a lower level than expected for a child’s age, such as language, motor, cognition, or play.
An encephalocele is a rare birth defect in which the tissue covering the brain, and a portion of the brain itself, protrude through openings in the skull.
Genetic disorders include certain types of birth defects, chronic diseases, developmental problems, and sensory deficits that are inherited from one or both parents.
Head injury is a broad term that describes many different types of conditions — ranging from bumps and bruises to concussions, skull fractures, and serious brain injuries.
“Learning disorder” and “specific learning disability” refer to a neurodevelopmental problem in which a child of normal intellectual potential is encountering unusual difficulty with their academic functioning that cannot be...
Multisystem inflammatory syndrome in children (MIS-C), also called pediatric multi-system inflammatory syndrome temporally related to SARS CoV-2 (PMIS or PIMS-TS), is a potentially serious illness in children that appears to...
Multiple sclerosis (MS) is when the body's immune system reacts against the central nervous system (CNS), which includes the brain, spinal cord, and optic nerves.
Relapsed neuroblastoma is when neuroblastoma returns in patients who have already undergone treatment for the disease. Refractory neuroblastoma is when the tumor does not respond to initial treatment.
Sanfilippo syndrome (aka mucopolysaccharidosis type III (MPS III)) is a rare, inherited disorder that's classified as a lysosomal storage disorder (LSD).
Sickle cell disease is an inherited blood disorder where cells cluster together, making it difficult for them to move through small blood vessels, thus denying oxygen to the blood.
Stroke is a general term that is used to describe an injury to the brain caused by either bleeding (referred to as hemorrhagic stroke) or a lack of oxygen due...
Tetralogy of Fallot (TOF) is a serious congenital heart defect where the heart’s anatomy prevents enough oxygen-poor (blue) blood from flowing to the lungs to receive oxygen.
Thumb hypoplasia means that your child’s thumb is unusually small or underdeveloped. Thumb aplasia means that your child’s thumb is missing altogether.