Literature DB >> 31563187

What to Do with an Abnormal Newborn Screen for Severe Combined Immune Deficiency.

Hey J Chong1, Scott Maurer2, Jennifer Heimall3.   

Abstract

Newborn screening for severe combined immunodeficiency has been implemented in all 50 states. This screening identifies newborns with T-cell lymphopenia. After an abnormal screening, additional testing is needed to determine if the child has severe combined immunodeficiency. Because screening programs vary, it is imperative for the clinical immunologist to understand how screening is done in their state and to prepare an effective assessment protocol for the management of these patients. Part of this assessment should include training and helping to ensure the effective delivery of this news to the family, a skill neither intuitive nor classically taught to immunologists.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Newborn screen; SCID screen protocol; Severe combined immunodeficiency

Mesh:

Substances:

Year:  2019        PMID: 31563187     DOI: 10.1016/j.iac.2019.07.007

Source DB:  PubMed          Journal:  Immunol Allergy Clin North Am        ISSN: 0889-8561            Impact factor:   3.479


  2 in total

1.  Retrospective Analysis of a New York Newborn Screen Severe Combined Immunodeficiency Referral Center.

Authors:  Melissa D Gans; Tatyana Gavrilova
Journal:  J Clin Immunol       Date:  2020-01-29       Impact factor: 8.317

2.  Trends in Pediatric Primary Immunodeficiency: Incidence, Utilization, Transplantation, and Mortality.

Authors:  Taylor Eddens; Molly Mack; Meghan McCormick; Hey Chong; Ramasubramanian Kalpatthi
Journal:  J Allergy Clin Immunol Pract       Date:  2021-10-27
  2 in total

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