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Services

PSGS Functions

Pediatric Screening and Genetic Services (PSGS), a unit within the Division of Child and Adolescent Health, provides the following functions.

PSGS Programs

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.

Virginia Genetics Program

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.

PSGS Special Projects

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.

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Pediatric Screening and Genetics Services

Contact: Nancy Ford
109 Governor Street, 8th Floor
Richmond, VA 23219
Phone: (804) 864-7691
Fax: (804) 864-7721

nancy.ford@vdh.virginia.gov

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Last Updated: 04-23-2008

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