811-820 of 4165 Results Found
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Trisomy 13 and Trisomy 18 in Children What are trisomy 13 and trisomy 18 in children? Trisomy 13 and trisomy 18 are genetic disorders. They include a combination of birth defects. This includes severe learning problems and health problems that affect nearly every organ in the
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Bronchopulmonary Dysplasia (BPD) Program When your baby’s health is on the line, you want the best care possible, and your baby deserves it. That’s why Phoenix Children’s established the Bronchopulmonary Dysplasia Program. We offer the most comprehensive …
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Turner Syndrome (Monosomy X) in Children What is Turner syndrome (TS) in children? Turner syndrome (TS) is a genetic disorder that occurs in girls. It causes many traits and problems. Girls with TS are shorter than most girls. They don’t go through normal puberty as they grow
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Cardiac Neurodevelopmental Program Many children with heart disease are at higher risk for long-term developmental, behavioral and psychological problems. As survival rates in children with cardiac disease continue to improve, it’s evident that this group …
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Diaphragmatic Hernia in Children What are diaphragmatic hernias in children? A diaphragmatic hernia is a birth defect that occurs in about 1 in 2,500 newborns. It happens in a baby during pregnancy. In this condition, there’s an opening in your baby’s diaphragm. This is the
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Specialty
At Phoenix Children’s Cardiology, our multispecialty team of experts works together to offer personalized care that ensures the best possible outcomes for everyone we serve. Whether a patient needs treatment for a complex heart condition, help managing an ongoing disorder or
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Thyroid Conditions Click on the links below to learn more about these topics. Hyperthyroidism Hypothyroidism Postpartum Thyroiditis© 2000-2025 The StayWell Company, LLC. All rights reserved. This information is not intended as a substitute for professional medical care. Always
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Cardiometabolic Risk Assessment, Research and Education (CARE) Program Email: care@phoenixchildrens.com Referrals Fax: 602-933-2436 Our CARE program is part of the Division of Endocrinology and Diabetes . We provide health education, promote the …
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Medical Genetics: Types of Genetic Changes The human body has about 20,000 different genes in each cell. Genes are located on chromosomes, which are stick-shaped structures in the middle of the cell (nucleus). Each cell usually has 46 chromosomes grouped in 23 pairs. Each gene
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Trinucleotide Repeats: Fragile X Syndrome What are trinucleotide repeats? DNA is the chemical that makes up your genes. It contains a "code" of 3-letter words known as codons or trinucleotides. Many genes normally contain trinucleotide sequences that repeat. These are called