Pediatric Genetics

Pediatric Genetics is committed to providing you, your newborn, children, or adolescents with excellent care in diagnosis, management and treatment of all forms of hereditary disorders and birth defects.  Our staff includes many specialists from clinical geneticists, counselors to neurologists that work as a team to develop your child’s treatment plan.

Schedule an Appointment: 

801-213-3599

Pediatric Genetic Services Offered: Metabolic Clinic Enzyme Replacement Therapy Fetal Alcohol Syndrome Newborn Screening Counseling and Education Pediatric General Evaluation Disorders of growth Neurocognitive impairment including autism Birth defects Distinctive facial features Hearing impairment (in conjunction with Otolaryngology)

Specific Expertise in: Neurofibromatosis (NF-1 & NF-2) Prader-Willi Syndrome Marfan Syndrome Down Syndrome Chromosome 22q11 Deletion Syndrome Turner Syndrome Chromosome Abnormalities

Locations

Primary Children's Medical Center (PCMC)	100 N Mario Capecchi Dr., Suite 2650 Salt Lake City, UT 84113 Map	(801) 213-3599
Utah Department of Health	44 N Mario Capecchi Dr. Salt Lake City, UT 84113	(801) 213-3599
Primary Children's Outpatient Services at Riverton	3773 West 12600 South Riverton, UT 84065 Map	(801) 213-3599

Bonnie J. Baty, CGC, M.S.

Specialties: Genetic Counselor, Pediatric Genetics

Steven B. Bleyl, M.D., Ph.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics

Lorenzo D. Botto, M.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics

John C. Carey, M.D., M.P.H.

Locations

PCMC Outpatient Services at Riverton	(801) 213-3599
Primary Children's Medical Center	(801) 213-3599

Specialties: Pediatric Genetics, Medical Genetics

Julie R. Korenberg, M.D., Ph.D.

Specialties: Pediatric Genetics

Susan O. Lewin, M.B.B.Ch.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics

Nicola Longo, M.D., Ph.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics, Medical Genetics

John M. Opitz, M.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics, Medical Genetics

Janice C. Palumbos, M.S.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Genetic Counselor, Pediatric Genetics

Alan F. Rope, M.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics

Sarah T. South, Ph.D.

Specialties: Pediatric Genetics

David A. Stevenson, M.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Hereditary Hemorrhagic Telangiectasia, Pediatric Genetics

David H. Viskochil, M.D., Ph.D.

Locations

PCMC Outpatient Services at Riverton	(801) 213-3599
Primary Children's Medical Center	(801) 213-3599
Utah Department of Health	(801) 581-8943

Specialties: Pediatric Genetics, Medical Genetics

Ashley Warnock, M.D.

Locations

Primary Children's Medical Center

(801) 213-3599

Specialties: Pediatric Genetics

Pediatric Clinical Trials

Sorry there are no trials related to this service

Related Documents

Pediatric Diseases and Conditions

• Autosomal Dominant: Marfan Syndrome
• Chance a Chromosome Abnormality Will Occur Again: Numerical, Structural (Inherited and De Novo), Mosaicism
• Chromosomal Abnormalities
• Chromosome Abnormalities
• Cystic Fibrosis Overview
• Down Syndrome (Trisomy 21)
• Fetal Alcohol Syndrome
• How Chromosome Abnormalities Happen: Meiosis, Mitosis, Maternal Age, Environment
• Marfan Syndrome
• Mosaic Down Syndrome
• Overview of Chromosome Abnormalities
• Overview of Single Gene Defects
• Single Gene Defects
• Structural Abnormalities: Deletions (Cri du Chat) and Duplications (Pallister Killian)
• Studies for Single Gene Defects: DNA (Direct and Indirect)
• Testing for Birth Defects
• The Difference Between a Chromosome Abnormality and a Single Gene Defect
• Translocation Down Syndrome
• Turner Syndrome
• Types of Chromosome Abnormalities
• Types of Genetic Diseases

News

• Alzheimer's Med Seems Ineffective in Those With Down Syndrome
• Apples Help Keep Muscles Strong, Mouse Study Finds
• Blood Test Detects Down Syndrome During Pregnancy
• 'Bubble Boy' Kids Living Normally After Gene Therapy: Study
• Can Blood Test Predict Breast Cancer Risk?
• Can Low Birth Weight Raise Autism Risk?
• Certain Genetic Regions May Be Tied to Osteoporosis
• Cheaper DNA Sequencing Coming Closer
• Common Breast Cancer Gene Test May Be Flawed, Study Says
• Counseling May Help Women at Risk for Breast Cancer Gene
• Daily Aspirin May Help Prevent Colon Cancer for Those at High Risk
• Doubt Cast on Use of Genetic Test Before Plavix
• Down Syndrome Brings Joy, Not Regrets, for Many Families
• EKG Testing May Spot Fatal Heart Conditions in Children
• Family Heart Disease Risk Linked to Genes, Not Lifestyle
• Family of Four Has Its Genome Sequenced
• Family Tree May Affect Diagnosis Age in Some Breast Cancers
• Family Tree May Aid Treatment of Inherited Heart Disorders
• Gene Behind Psoriasis Identified, Researchers Say
• Gene Linked to Separation Anxiety
• Gene Linked to Start of Puberty
• Gene Mutation Can Leave People Without Fingerprints
• Gene Mutation May Be Key to Familial Pancreatic Cancer
• Gene Mutations Linked to Thyroid Cancer Risk: Study
• Gene Sequencing Helps Twins With Rare Disorder
• Gene Study Identifies Non-Hereditary Links to Schizophrenia
• Gene Study Sheds Light on Often Fatal Heart Condition
• Gene Tests May Not Drive Patients to More Medical Care
• Gene Therapy a Boon for 6 Hemophilia Patients
• Genes Associated With Autism Also Related to Schizophrenia
• Genes Linked to Restless Legs Syndrome Identified
• Genetic Test May Spot Raised Autism Risk
• Genome Map Might Help Save Tasmanian Devil From Extinction
• Girls May Be More Resistant to Autism Than Boys: Study
• Gluten-Free Set This Boy Free
• Healthy Diet May Counteract Heart Disease Gene
• In Mice, Drug Reverses Symptoms of Condition Linked to Autism
• Many Doctors Ignore Cancer Genetic Testing Guidelines
• Maternal Blood Test Can Determine Sex of Fetus at 7 Weeks
• Maternal Blood Test Might Spot Birth Defects More Safely
• Most Parents Tell Kids About Test Results for Breast Cancer Genes
• Mutant Gene That Ups Risk for Ovarian Cancer May Aid Survival
• Mutations in 2 Genes Linked to Rare Autism-Related Disorder
• New Approach to Treating Asthma in Pregnancy
• Older Dads Can Pass on Gene Mutations That Lower Intellect
• Possible Genetic Link to Autism Identified
• Researchers Find 3 Genes Linked to Esophagus Disorders
• Researchers Find Gene Mutations That May Be a Key to Autism
• Researchers Find Link Between Epilepsy, Schizophrenia Risk
• Researchers ID Gene for Neck Disorder
• Scientists Discover Key Gene Mutation Behind Lou Gehrig's Disease
• Scientists Find Molecular Similarities in Brains of Those With Autism
• Scientists ID Gene Linked to Syndrome Behind Elephant Man Disease
• Scientists ID More Genes Linked to Heart Disease
• Scientists Identify Genes Linked to Migraines
• Scientists May Have Found Missing Link to Common Brain Cancer
• Scientists Pinpoint Childhood Obesity Genes
• Screening Alone Not Enough to Prevent Sudden Death in College Athletes
• Some Causes of Stillbirth May Be Avoidable: Studies
• Study: Inherited Alzheimer's Detectable 20 Years Before Symptom Onset
• U.S. Scientists Map Genome of Advanced Prostate Cancer
• Women With BRCA Mutations Get Cancer Diagnosis Earlier Than Before