| Literature DB >> 25677830 |
K Golden-Grant1, J L Merritt2, C R Scott2.
Abstract
Population-based genetic screening has been a mainstay of public health in the United States for many years. The goal of genetic screening is to identify individuals at increased risk for treatable diseases. The evolution of genetic testing to include multi-disease panels allows for new screening applications which challenge the traditional model of clinical genetics care by the identification of late-onset disorders in an asymptomatic fetus, child, or adult. We present two unique examples of individuals referred to a biochemical genetics clinic due to the detection of late-onset Pompe disease by population-based screening modalities. We review early experiences in counseling and management of pre-symptomatic individuals and highlight some of the primary ethical factors warranting consideration as we enter the era of genomic medicine.Entities:
Keywords: Pompe disease; autonomy; beneficence; ethics; genetic screening; justice; newborn screening; next-generation sequencing; non-maleficence
Mesh:
Year: 2015 PMID: 25677830 DOI: 10.1111/cge.12566
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438