This review aimed to develop a framework to understand the process of information
management in families with inherited conditions. Electronic databases were searched for …

Background Individuals with BRCA1/2 mutations have a notably higher than average
lifetime risk of developing cancer as adults. Some parents with BRCA1/2 mutations wish to …

Low uptake of genetic services among members of families with hereditary breast and
ovarian cancer (HBOC) suggests limitations of proband-mediated communication of genetic …

Cascade genetic testing of relatives from families with pathogenic variants associated with
hereditary breast and ovarian cancer (HBOC) or Lynch syndrome (LS) has important …

Objective The goal was to explore how families communicate to cope with hereditary cancer
conditions and identify factors that may enhance resilience and recommended decision …

Objective The present review describes how children experience hereditary cancer risk
communication within the family. Methods Searches for studies between 1990 and 2020 on …

The limited literature on Asian family communication of hereditary cancer risk and cascade
genetic testing for pathogenic variants (PVs) in BRCA1 and BRCA2 has reported that Asian …

Objective We examined how responsibility (the “duty to inform relatives about genetic testing
results”) is understood and enacted among Swiss and Korean women carrying BRCA1 or …

This scoping review sought to examine the existing literature on multifamily interventions
with families dealing with inherited genetic conditions. It also seeks to identify gaps in the …

As the number of people with cancer increases, so does the number of informal caregivers.
These caregivers frequently have multiple unmet needs and experience numerous burdens …