
Pediatric Screening and Genetic Services (PSGS), a unit within the Division of Child and Adolescent Health, provides the following functions.
Virginia Early Hearing Detection and Intervention Program
The goal of the Virginia Newborn Hearing Screening Program is to achieve identification of congenital hearing loss in children by three months of age and to assure enrollment in appropriate intervention by six months of age.
The goal of the Virginia Genetics Program is to maintain a statewide system of services to reduce unnecessary infant death and disabilities from potential or existing geneticconditions. It does this by providing Virginia residents with information, testing, counseling, and treatment.
Virginia Child Health Information Systems Integration Project (Virginia CHISIP)
CDC Cooperative Agreements for Early Hearing Detection and Intervention (EDHI) Tracking, Surveillance, and Integration.
Virginia Infant Screening and Infant Tracking System (VISITS)
A secure Web-based integrated tracking and data management system that supports the following programs and services:
Virginia Congenital Anomalies Tracking and Prevention Project (Virginia CATPIP)
CDC Cooperative Agreements for the Development and Improvement of Population-Based Birth Defects Surveillance Programs and the Integration of Surveillance Data with Public Health Programs.
Pediatric Screening and Genetics Services
Contact: Nancy Ford
109 Governor Street,
8th Floor
Richmond, VA 23219
Phone: (804) 864-7691
Fax: (804) 864-7721