Dr. Victoria Evans Judd MD
Cardiologist (Pediatric) | Pediatric Cardiology100 N Medical Dr Salt Lake City UT, 84113
Dr. Victoria Judd is a pediatric cardiologist practicing in Salt Lake City, UT. Dr. Judd specializes in caring for fetuses, infants, children and adolescents with cardiovascular or cardiac abnormalities. Practiced in both inpatient and outpatient settings, the scope of conditions cared for by pediatric cardiologists is large and includes congenital heart defects, heart muscle disorders, rhythm disturbances and hypertension.
PediatricsAmerican Board of PediatricsABP- Pediatric Cardiology
Expert PublicationsData provided by the National Library of Medicine
- Supraventricular tachycardia in infancy: evaluation, management, and follow-up.
- Spontaneous resolution of ventricular arrhythmias with left bundle branch block morphology and abnormal endomyocardial biopsy.
- Demographic characteristics of US medical school admission committees.
- Double balloon technique for dilation of valvular or vessel stenosis in congenital and acquired heart disease.
- Noninvasive imaging techniques.
- Prospective evaluation of the antenatal incidence and postnatal significance of the fetal echogenic cardiac focus: a case-control study.
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Patient Experience with Dr. Judd
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Kawasaki disease is a rare childhood disease that causes inflammation of the arteries in the body. The characteristic symptoms of the disease, which is high fever and peeling skin, remains for almost a week. In most cases, it gets back to normal without any major issues. Children will be monitored...
- Newborn Diagnosis: Tetralogy of Fallot
Tetralogy of FallotTetralogy of Fallot is a congenital heart defect, which affects the heart’s structure, causing blood with low levels of oxygen to circulate throughout the body. Babies born with tetralogy of Fallot tend to have a blue discoloration of the skin due to low oxygen levels in their...
- What Is Neonatal Lupus?
Neonatal lupus is a not so common autoimmune disease. It is not true lupus as all the symptoms will completely disappear after 6 months of age. Neonatal lupus is also known by several other terms. The condition is also called as:...
- What Is Progeria?
Progeria or Hutchinson-Gilford progeria syndrome (HGPS), is a rare genetic condition characterized by a rapidly aging appearance in children. Newborns and infants born with this condition typically look healthy and normal, but may physically display characteristic facial features, such as prominent...
- What Is Duchenne Muscular Dystrophy? Causes, Symptoms, and Treatment
Muscular dystrophies are a group of diseases that make the muscles of the body weaker over a period of time. The muscles become less flexible in this condition. Out of the nine types of muscular dystrophy, Duchenne muscular dystrophy is one of the most common.The main characteristics of this medical...
- Muscular Dystrophy: Telling a Child the Truth About His/Her Condition
Muscular dystrophy is a category of muscle diseases that cause progressive weakness and loss of muscle mass. Muscular dystrophy (MD) is either inherited or can be due to a genetic mutation. Kids with MD usually follow a normal pattern of growth development in the first few years of their lives,...
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