Author

Emmanuel Miller Page 4

At an outpatient pediatric genetics clinic in Park City, Utah, Emmanuel Miller, PA-C, evaluates infants and young children with rare congenital conditions and coordinates their ongoing specialty care. He has worked in clinical genetics for 20 years, conducting diagnostic reviews and helping families organize multidisciplinary treatment plans across pediatric neurology, cardiology, and metabolic therapy services. Miller received a Bachelor of Science in Biology from the University of New Hampshire and finished a Master of Science in Physician Assistant Studies. In addition to his hospital-affiliated clinical duties, he contributes educational articles on rare genetic syndromes to Biology Insights.

3-MCC Deficiency: Causes, Symptoms, and Treatment Hormones
What Are HSR Elements and How Do They Affect Cancer?Cancer
CHH Dwarfism: Causes, Symptoms, and Medical Management Hormones
PTPN11’s Role in Noonan Syndrome: Causes and Symptoms Genetics
Van Maldergem Syndrome: Physical Traits, Diagnosis, and Care Genetics
Burnside Butler Syndrome: Genetic Roots and Clinical Indicators Genetics