Conditions We Treat

Browse Conditions A-Z

22q Deletion Syndrome

22q11.2 deletion syndrome, also known as DiGeorge Syndrome, is a condition where there is a small amount of genetic material missing (a microdeletion) on the long arm (the q arm) of chromosome 22. 22q has the potential to impact every system in the body and can lead to a range of health issues.

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22q11.2 Deletion Syndrome in Children

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.

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A Child Living with a Pacemaker or Implantable Cardioverter Defibrillator (ICD)

Detailed information on living with a pacemaker or implantable cardioverter defibrillator

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Abdominal Pain

Functional abdominal pain is a common problem that interferes with a child’s daily life. Some red flags to look for include weight loss, vomiting, lack of energy and bloody diarrhea. A physician can perform tests to determine the cause of abdominal pain. Treatment plans vary depending on the cause.

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Abdominal Pain: Outpatient

In this Helping Hand™ document, we discuss what steps to take if the cause of your child's abdominal pain cannot be determined. It is important that you watch your child closely for the next 24 hours and go back to your child’s doctor or the emergency department if they show more serious symptoms.

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About Poison Control Centers

Poison control centers are always open - 24 hours a day, 7 days a week, 365 days a year. They're staffed by pharmacists, healthcare providers, nurses, and other experts who are available by phone.

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About the Heart and Blood Vessels

Detailed anatomical description of the heart's blood vessels, including simple definitions and a labeled, full-color illustration

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Abrasions

An abrasion is a superficial rub or wearing off of the skin, usually caused by a scrape or a brush burn. Abrasions are usually minor injuries that can be treated at home.

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Acanthosis Nigricans

Acanthosis nigricans (AN) is a dark patch that appears on a child's neck, armpit, under the breast or a skin crease. It is usually a sign that the body is making extra insulin that it cannot use well. Eating a healthy diet and increasing physical activity are steps to help cure acanthosis nigricans.

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Achalasia in Children

Achalasia is a rare disease that makes it hard to swallow foods and liquids. In achalasia, there is a problem with the tube that carries food from the mouth to the stomach (esophagus).

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Achondroplasia

Achondroplasia is the most common form of short-limb dwarfism. Individuals who have achondroplasia have short limbs but normal trunk height and head size with a prominent forehead. Children with achondroplasia can lead normal lives provided they receive appropriate care by knowledgeable providers.

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Achondroplasia in Children

Achondroplasia is a group of rare genetic (inherited) bone disorders. Achondroplasia is the most common type of what was once called dwarfism, in which the child's arms and legs are short in proportion to body length.

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Helping Hands Patient Education Materials

Written and illustrated by medical, nursing and allied health professionals at Nationwide Children's Hospital, Helping Hand instructions are intended as a supplement to verbal instructions provided by a medical professional. The information is periodically reviewed and revised to reflect our current practice. However, Nationwide Children's Hospital is not responsible for any consequences resulting from the use or misuse of the information in the Helping Hands.