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Pediatrics (Evanston), 2019-01, Vol.143 (Suppl 1), p.S27-S32
2019
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Details

Autor(en) / Beteiligte
Titel
Challenging the Current Recommendations for Carrier Testing in Children
Ist Teil von
  • Pediatrics (Evanston), 2019-01, Vol.143 (Suppl 1), p.S27-S32
Ort / Verlag
United States
Erscheinungsjahr
2019
Quelle
MEDLINE
Beschreibungen/Notizen
  • The authors of current professional guidelines generally do not support the return of information about genetic carrier status for infants and children because of a perceived lack of immediate benefit and an abundance of caution regarding potential harm and desire to protect the children's future autonomy. The advent of genomic sequencing, used either as a diagnostic or a screening tool, and the increasing use of this technology in childhood creates the potential for the identification of carrier status in the pediatric period. As part of the BabySeq Project, researchers are exploring the implications of genomic sequencing in both newborns who are healthy and newborns who are sick and developing policies and procedures for the return of carrier status information to the parents and physicians of newborns. In this commentary, we review the history of carrier testing in children and explore the potential benefits, risks, and challenges of returning such results both for the children, their parents, and potential future siblings.
Sprache
Englisch
Identifikatoren
ISSN: 0031-4005
eISSN: 1098-4275
DOI: 10.1542/peds.2018-1099F
Titel-ID: cdi_pubmed_primary_30600268

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