Referral required from primary physician. Open to individuals of all ages with a wide range of genetic conditions.

Provides genetic counseling and consultation for conditions including chromosomal disorders, single gene disorders and recognizable syndromes. 

Services Include:

• Metabolic clinic
• Lysosomal storage disorders clinic
• Fetal alcohol syndrome
• Newborn screening counseling & education
• Pediatric general evaluation
  • Disorders of growth
  • Neurocognitive impairment including autism
  • Birth defects
  • Distinctive facial features
  • Hearing impairment (in conjunction with otolaryngology)

Conditions and Treatments:

• Neurofibromatosis (NF1 & NF2)
• Prader-Willi Syndrome
• Marfan syndrome
• Down syndrome
• Chromosome 22q11
• Deletion syndrome
• Turner syndrome
• Chromosome abnormalities

Patients also be seen at Primary Children's Hospital Outpatient Services at Riverton.

Provides complete prenatal diagnostic services. This includes the following:

• 2D and 3D/4D ultrasound imaging
• Fetal MRI and invasive testing by amniocentesis
• Chorionic villus sampling

Offers complete genetic counseling services to educate patients and their families about their prenatal testing options. This may include the risk of having a child with a birth defect or genetic disease.

Conducts research into various possible causes of autism spectrum disorders. Part of a larger networks in the US and Europe, including the Autism Sequence Consortium and the Autism Genome Project.

Individuals with autism spectrum disorder or other childhood developmental disorders. Any age.

Offers customized genetic testing service for individuals with autism spectrum disorder (ASD) and other disorders of childhood development plus ASD, multiple sclerosis (MS), and chronic obstructive pulmonary disease (COPD).

Lineagen, Inc. is a privately held personal genomics and biotechnology company based in Salt Lake City.

Provides care to optimize the health of patients and families affected by congenital anomalies, both during pregnancy and after birth, and to improve available treatment. Includes maternal fetal medicine specialists for the pregnant mother, neonatologists who are specially trained to care for newborns, and pediatric specialists for all your baby’s needs before and after delivery.

Stephen Fenton, MD, Director

Provides information about Duchenne Muscular Dystrophy for families, including responding to a new diagnosis, finding care, and genetic testing. PPMD’s Decode Duchenne genetic testing program provides free genetic testing and counseling to people in the Duchenne or Becker muscular dystrophy community who otherwise could not afford genetic testing.

Runs Certified Duchenne Care Center Program, which supports standardized comprehensive care for people with Duchenne. Also promotes research and organizes advocacy initiatives.

Provides research.

An online database for pediatric genetics centers, containing the locations of genetics clinics that have requested to be listed.
Check Pediatric Genetics under "Search by genetic service type(s)”.

American College of Medical Genetics and Genomics (ACMG)

The National Society of Genetic Counselors (NSGC) promotes the professional interests of genetic counselors and provides a network for professional communications. Access to continuing education opportunities, professional resources, advocacy and the discussion of all issues relevant to human genetics and the genetic counseling profession are an integral part of belonging to the NSGC.

[https://www.nsgc.org/page/find-a-genetic-counselor Find a Genetic Counselor].

Tests kits can be ordered by individuals or a medical provider. Accepts private pay. Will bill to insurance if requested and Patient Assistance is available by application.

Provides a variety of in-home saliva genetic testing options.

Provides telephone-based genetic counseling services to patients, clinical providers and organizations in all 50 states.

Provides telephone-based genetic counseling services.