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PO Box 360
Trenton, NJ 08625-0360

For Release:
November 17, 2008

Heather Howard
Commissioner

For Further Information Contact:
S. Patricia Cabrera
(609) 984-7160


 
Department of Health and Senior Services Proposes New Rules and Amendments at N.J.A.C. 8:20, which establishes the Birth Defects Registry


 

       The Division of Family Health Services in the Public Health Services Branch of the Department of Health and Senior Services proposes new rules and amendments at N.J.A.C. 8:20, which establishes the Birth Defects Registry.

 

       The proposal would establish an autism registry and a severe neonatal jaundice registry.

 

       This proposal would require health care professionals to report diagnoses of autism in children from birth through twenty-one years of age.  N.J.S.A. 26:2-187 requires the Department of Health and Senior Services to implement the reporting of autism and to establish an autism registry. Autism is a developmental disorder of brain function that is typically manifested by impaired social interaction, problems with verbal and nonverbal communication and imagination, and unusual or severely limited activities and interests. 

 

       Under the proposal, health care professionals would not report the personal identifying information of a child diagnosed with autism if the child’s parent, legal guardian or custodian objects to the reporting of this information, or if the individual through age twenty-one who is diagnosed with autism objects to the reporting.  Health care professionals would be required to inform the parent, legal guardian, custodian or individual through age twenty-one of the right to refuse to report identifying information.

 

       The proposal would require clinical laboratories to report newborns with severe neonatal jaundice, a condition that is caused by a buildup of bilirubin, an orange-yellow pigment found in bile.  Toxic levels of bilirubin can cause severe neurological damage called kernicterus.  N.J.S.A. 26:8-40.21 requires the Department to establish a severe neonatal jaundice registry.

 

       The proposal would also make the reporting requirements for congenital conditions more consistent with the Centers for Disease Control and Prevention (CDC) Guidelines, and extend the reporting requirements for congenital conditions from birth through five years of age.

 

       Under the proposal, the information on individuals with these conditions that is reported to these registries would remain confidential.  The data contained in these registries would be used for public health research, needs assessments, and public health investigations.

 

       The notice of proposal appears in the November 17, 2008 issue of the New Jersey Register.

 

       The public has until January 16, 2009 to comment on the proposals.  Persons wishing to comment on the proposals must submit their comments in writing to Ruth Charbonneau, Director, Office of Legal and Regulatory Affairs, New Jersey Department of Health and Senior Services, PO Box 360, Trenton, NJ 08625.  Written comments on the proposals must be postmarked on or before January 16, 2009, which is the close of the 60-day public comment period for the proposals.

 

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