1. Home
  2. UT Services Directory
  3. Fetal Alcohol Spectrum Disorders Clinics (2)

Fetal Alcohol Spectrum Disorders Clinics

Provide Feedback
Suggest a New Provider

A clinic specializing in treatment of individuals with Fetal Alcohol Spectrum Disorders, a continuum of permanent birth defects caused by maternal consumption of alcohol during pregnancy, the effects of which can include physical problems and problems with behavior and learning. (Adapted from AIRS YF-3000.2120)

Service Legend
Local Service
Statewide Service: Provides online resources, telehealth, or service at a satellite office.
Nationwide Service: Provides online resources, telehealth or services at a regional/national headquarters location.
Pediatric Medical Genetics, University of Utah Health- Department of Pediatrics View on Map
81 North Mario Capecchi Drive
Eccles Primary Children's Hospital Outpatient Services Building
Salt Lake City, UT 84113
 Phone: 801-213-3599
Organization Name: University of Utah Health- Department of Pediatrics
(Show others in Organization)
Address:
81 North Mario Capecchi Drive
Eccles Primary Children's Hospital Outpatient Services Building
Salt Lake City, UT 84113
Phone: 801-213-3599
Fax: 801-585-7252
Service Categories:
Biochemical Genetics (Metabolics)
Biochemical Genetics (Metabolics) Clinics
Fetal Alcohol Spectrum Disorders Clinics
Genetic Testing and Counseling
Medical Genetics
Medical Genetics Clinics
Neurofibromatosis Clinics
URL: https://healthcare.utah.edu/pediatrics/programs-services/genetics.php
Wheelchair Access: Yes
Eligibility:

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

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
Source: Medical Home Portal
Last Updated: 12/22/2021
Show more details ...
Pediatric Medical Genetics, University of Utah Health- Department of Pediatrics View on Map
3773 West 12600 South
Primary Children's Hospital Outpatient Services at Riverton
Riverton, UT 84065
 Phone: 801-213-3599
Organization Name: University of Utah Health- Department of Pediatrics
(Show others in Organization)
Address:
3773 West 12600 South
Primary Children's Hospital Outpatient Services at Riverton
Riverton, UT 84065
Phone: 801-213-3599
Fax: 801-585-7252
Service Categories:
Biochemical Genetics (Metabolics)
Biochemical Genetics (Metabolics) Clinics
Fetal Alcohol Spectrum Disorders Clinics
Genetic Testing and Counseling
Medical Genetics
Medical Genetics Clinics
Neurofibromatosis Clinics
URL: https://healthcare.utah.edu/pediatrics/programs-services/genetics.php
Wheelchair Access: Yes
Eligibility:

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

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
Source: Medical Home Portal
Last Updated: 12/22/2021
Show more details ...