Develops new laboratory methods to identify babies with SCID,.Provides training and technical assistance to state labs screening for SCID,.Funds SCID test development and early screening in collaboration with states,.In an effort to expand and improve screening, CDC's Division of Laboratory Sciences: Since 2008, CDC has worked to increase the number of U.S states and territories that include accurate SCID testing as part of their newborn screening programs. WI and MA identified more than 10 cases of SCID and more than 40 cases of other immune deficiencies using SCID newborn screening. This baby was successfully treated and is now living a healthy life. Wisconsin lab identified the first SCID baby with the help of CDC funded newborn screening! SCID was added to the core Recommended Uniform Screening Panel (RUSP) in 2010. Although each state decides which disorders are included in the screening, the Secretary's Advisory Committee on Heritable Disorders in Newborns and Children (SACHDNC) recommends states test for a core panel of 31 congenital disorders2. The blood sample is sent to a state laboratory to be tested for several severe disorders. Shortly after a baby is born, a health professional takes a few drops of blood from the baby's heel. CDC's Division of Laboratory Sciences has developed laboratory tests and reference materials for SCID using dried bloodspots and is working to advance screening nationwide. for numerous diseases, and 32 states and the District of Columbia currently screen for SCID. Nearly 4 million newborns are screened annually in the U.S. Newborn screening identifies babies with congenital disorders like SCID. If SCID is diagnosed early in life, before the onset of infection, a bone marrow transplant can successfully treat the disorder. They may die before 1 year of age without medical treatment1. Severe Combined Immunodeficiency (SCID) Importance of Newborn Screening for SCIDÄ«abies born with Severe Combined Immunodeficiency (SCID) appear normal at birth but cannot fight infection.
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