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What to Do with an Abnormal Newborn Screen for Severe Combined Immune Deficiency.
Chong, Hey J; Maurer, Scott; Heimall, Jennifer.
Afiliação
  • Chong HJ; Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA 15224, USA. Electronic address: hey.chong@chp.edu.
  • Maurer S; Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA 15224, USA.
  • Heimall J; Division of Allergy and Immunology, Children's Hospital of Philadelphia, Wood 3301, 3401 Civic Center Boulevard, Philadelphia, PA 19104, USA.
Immunol Allergy Clin North Am ; 39(4): 535-546, 2019 11.
Article em En | MEDLINE | ID: mdl-31563187
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa Idioma: En Ano de publicação: 2019 Tipo de documento: Article