Information for parents about trisomy 18, a rare genetic condition that causes developmental delay and affects many different organ systems.
Information for parents about trisomy 13, a rare genetic condition that causes developmental delay and affects many different organ systems.
Down syndrome is a genetic condition present at birth. Learn about the symptoms, complications and outlook for children with Down syndrome.
Learn about the role that genetics plays in many heart conditions that afflict children.
Learn about how acute myeloid leukemia (AML) develops and what factors may affect the development of the disease.
Provides information about Asperger syndrome, which is a type of autism.
Read about the causes, symptoms, and treatments for Landau-Kleffner syndrome epilepsy, a rare condition in which children have difficulty with speech.
Marfan syndrome is a rare hereditary disorder of connective tissue. About 60% to 80% of people with this syndrome have heart problems.
Most children with Williams syndrome have a heart or blood vessel problem.
Read about the causes and symptoms of Lennox-Gastaut syndrome epilepsy and how the condition is treated.
The effects of CHARGE syndrome differ from one child to the next. Find out how this genetic condition is caused and treated.
Learn about heart-related syndromes. A syndrome is a medical term for a collection of signs and symptoms that generally stem from a single cause.
Noonan syndrome is a genetic condition. Learn about the symptoms and diagnosis of Noonan syndrome and the heart conditions associated with the condition.
Insulin resistance often accompanies polycystic ovary syndrome (PCOS). Learn more about how PCOS can lead to the development of type 2 diabetes.
Learn about hypoplastic left heart syndrome (HLHS). This condition involves the left side of the heart being underdeveloped, and is extremely serious.
Children with Down syndrome may be at a higher risk for some medical conditions. Learn what these conditions are and how to manage them.
Learn about multisystem inflammatory syndrome in children (MIS-C), a rare syndrome linked to a SARS-CoV-2 infection.
Nephrotic syndrome is one of the most common kidney diseases in children. It presents as a group of symptoms, which occur together in the body and include the presence of protein (albumin) in the urine and edema (swelling).
Polycystic ovaries syndrome (PCOS) is a disorder caused by hormonal imbalance. Learn about the effects of PCOS as well as possible treatment options.
An overview of the causes, symptoms and complications of Turner syndrome.
22q11 deletion syndrome (22q11DS) is a genetic condition. Learn what causes it, how it's diagnosed and treated.
Learn about the genetic causes of 22q11 deletion syndrome, risk factors and confirming diagnosis.
Learn about flat head syndrome and how it is treated.
Learn about single ventricle anomalies. This term refers to a group of severe conditions in which only one ventricle is of adequate size, such as hypoplastic left heart syndrome (HLHS).
Find out the causes and symptoms of Rasmussen syndrome and how this form of epilepsy is treated.
