Skip to main content
Global Menu
  • Urgent Care Scheduling & ER Wait Times
  • Patient Portal
  • Pay a Bill
  • Refer A Patient
  • Careers
  • Donate
Phoenix Children's Hospital Phoenix Children's Hospital
Main Navigation (Top)
Schedule an Appointment Find a Doctor Find a Location Find a Specialty
Search Phoenix Children's
Popular Links
Urgent Care Scheduling & ER Wait Times Patient Portal Pay a Bill Find a Doctor Locations Specialties & Conditions For Healthcare Professionals Careers
Main Navigation (Top)
Schedule an Appointment Find a Doctor Find a Location Find a Specialty
Hamburger Main
Patient & Visitor Information
Visitor Protocol
Planning Your Visit
Planning Your Stay
After Your Visit
Imaging & Radiology
Patient & Family Services
Support Programs
Educational Resources
Specialties & Conditions
Specialties
Services
Conditions
Pediatric Primary Care
Phoenix Children's Pediatrics
Primary & Complex Care
Phoenix Children's Care Network (PCCN)
Articles and FAQs
News
Blog
Patient Stories
FAQs
Research
Programs & Services
Research Areas of Focus
News & Innovation
Find a Research Study
For Healthcare Professionals
Patient Referrals
Clinical Pathways
Continuing Medical Education (CME)
Medical Education
Medical Staff
Nursing
Phoenix Children's Care Network (PCCN)
About Us
Awards & Recognition
Careers
Contact
Events - Healthcare Professionals
Healthcare Outreach
History of Phoenix Children's
Leadership Team
Newsroom - Media Guidelines
Phoenix Children’s Hospital Foundation
Ways to Help
Main Navigation (Bottom)
Patient Family Healthcare Professional Career Seeker
Urgent Care Scheduling & ER Wait Times Patient Portal Pay a Bill Request Medical Records Refer a Patient Donate Careers

Search Results

  • All
  • Services
  • Conditions
  • Doctors
  • Locations
  • Articles
3481-3490 of 4332 Results Found
Condition
Uniparental Disomy: Prader-Willi Syndrome and Angelman Syndrome
Uniparental Disomy: Prader-Willi Syndrome and Angelman Syndrome What is uniparental disomy? Chromosome pairs affect how our body works. Normally, a baby gets one copy of each chromosome pair from each birth parent. In rare cases, two copies come from the same parent. This is
Condition
Glomerulonephritis in Children
Glomerulonephritis in Children What is glomerulonephritis in children? The kidneys contain many coils of tiny blood vessels. Each of these is called a glomerulus. Glomeruli filter substances from the blood into the urine. Glomerulonephritis is a type of kidney disease where these
Condition
Hydrocele in Children
Hydrocele in Children What is a hydrocele in children? A hydrocele is fluid buildup in the thin pouch that holds the testes in the scrotum. Up to 1 in 10 baby boys have a hydrocele at birth. In most cases, it goes away without treatment in the first year. What causes a hydrocele
Condition
Inguinal Hernia in Children
Inguinal Hernia in Children What is an inguinal hernia in children? A hernia occurs when a part of the intestine or other abdominal tissue pushes through a weakness in the belly (abdominal) muscles. A soft bulge shows up under the skin where the hernia is. A hernia in the groin
Condition
Megaureter in Children
Megaureter in Children What is megaureter in children? Megaureter is a ureter that is much wider than normal. The ureters are the tubes that carry urine from the kidneys to the bladder. A ureter that is wider than 3/8 inch is a megaureter. A megaureter may not drain urine
Condition
Neurogenic Bladder in Children
Neurogenic Bladder in Children What is neurogenic bladder in children? Neurogenic bladder means the bladder doesn't work normally because of nerve damage. It causes a child to have problems with holding or releasing urine. The muscles and nerves of the urinary system work
Condition
Polycystic Kidney Disease
Polycystic Kidney Disease What is polycystic kidney disease (PKD)? Polycystic kidney disease (PKD) is a rare genetic disorder. It causes many cysts filled with fluid to grow in the kidneys. PKD cysts can impair how the kidneys work. It can lead to kidney failure. PKD is the
Condition
Genetic Disorders Associated with Congenital Heart Disease
Genetic Disorders Associated with Congenital Heart Disease Click on the links below to learn more about these topics. Down Syndrome Marfan Syndrome 22q11.2 Deletion Syndrome© 2000-2026 The StayWell Company, LLC. All rights reserved. This information is not intended as a
Condition
Maternal and Fetal Testing Overview
Maternal and Fetal Testing Overview Most people have healthy pregnancies, and their babies are born without trouble. But if you have a high-risk pregnancy, you may need to be closely watched for possible problems. There are tests and procedures that can help keep track of your
Condition
Cystic Fibrosis Overview
Cystic Fibrosis Overview What is cystic fibrosis? Cystic fibrosis (CF) is an inherited disease of the glands that make mucus and sweat. People with CF get a defective gene from both parents. People who have one defective gene from one parent are called carriers. They don't have

Pagination

  • Previous page
    Prev
  • First page 1
  • …
  • Page 348
  • Current page 349
  • Page 350
  • …
  • Last page 434
  • Next page
    Next
Phoenix Children's Hospital
Footer
  • Contact Us
  • Scheduling: 602-933-5437
  • Phone Directory
  • About Us
  • Manage Cookie Preference
Footer Right
  • Careers
  • Bright Futures Blog
  • Price Transparency
  • Phoenix Children’s Foundation
  • Facebook
  • Instagram
  • Youtube
  • LinkedIn
  • X
©2026 

Phoenix Children's. All Rights Reserved. | Our Policies

USNWR badge for 2026-2027
Picture of a cactus with sun and clouds