Carrier testing in children: exploration of genetic health professionals’ practices in Australia
Author(s) -
Danya F. Vears,
Clare Delany,
Lynn Gillam
Publication year - 2014
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1038/gim.2014.116
Subject(s) - genetic testing , carrier testing , genetic counseling , medicine , anxiety , health professionals , sibling , test (biology) , family medicine , health care , psychology , developmental psychology , psychiatry , genetics , biology , pregnancy , fetus , paleontology , prenatal diagnosis , economics , economic growth
Despite genetic health professionals routinely providing carrier testing in adults, carrier testing in unaffected children after a sibling is diagnosed with a genetic condition remains controversial. The majority of international guidelines addressing genetic carrier testing in children recommend against providing this testing, yet little is known about current practice. This study aimed to determine whether genetic health professionals receive requests for carrier testing in unaffected children from parents of children with genetic conditions and whether they provide this testing.
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