Dr. Anthony A. Catanzano

I am a clinical geneticist and a pediatrician with a deep interest in undiagnosed and rare genetic disorders. I provide medical care for children and adults with chromosome 22q11.2 deletion syndrome and diagnostic evaluation for patients with symptoms and signs of genetic disorders, when evaluations have not provided a specific diagnosis. Dr. Shashi is rated as a Distinguished provider by MediFind in the treatment of Acromicric Dysplasia. Her top areas of expertise are DiGeorge Syndrome, Hypotonia, Immune Defect due to Absence of Thymus, and Micrognathia.

Arthur Aylsworth is a Pediatrics provider in Chapel Hill, North Carolina. Dr. Aylsworth is rated as an Advanced provider by MediFind in the treatment of Acromicric Dysplasia. His top areas of expertise are Arthrogryposis Multiplex Congenita, Hypochondroplasia, Micrognathia, and Early Infantile Epileptic Encephalopathy.

I specialize in diagnosing and treating heritable arrhythmia syndromes that affect children and young adults such as long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia syndrome, and short QT syndrome. I specialize in identifying the cause of patients who have experienced a sudden cardiac arrest. I am a physician-scientist and cross-trained in pediatric cardiology, electrophysiology, human genetics, and molecular physiology. I lead an active research program that brings together clinical medicine, functional genomics, precision medicine, and molecular and cellular biology. Dr. Landstrom is rated as a Distinguished provider by MediFind in the treatment of Acromicric Dysplasia. His top areas of expertise are Cardiomyopathy, Wildervanck Syndrome, Holt-Oram Syndrome, and Alternating Hemiplegia of Childhood.