Individual and family characteristics associated with BRCA1/2 genetic testing in high-risk families

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Individual and family characteristics associated with BRCA1/2 genetic testing in high-risk families.

BACKGROUND Little is known about family members' interrelated decisions to seek genetic testing for breast cancer susceptibility. METHODS The specific aims of this cross-sectional, descriptive, cohort study were (i) to examine whether individual and family characteristics have a direct effect on women's decisions to use genetic testing for hereditary susceptibility to breast cancer and (ii) t...

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Cerebrotendinous xanthomatosis (CTX) is a rare inborn lipid-storage disease leading to a progressive multisystem disease. CTX with autosomal recessive inheritance is caused by a defect in the CYP27A1 gene. Hallmark clinical manifestations of CTX include bilateral cataracts, chronic diarrhea, tendon xanthomas, and neurologic dysfunction. CTX is a rare disorder, which is supposed to be under-diag...

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Objective: The aim of this study was to determine the effectiveness of structural family therapy in therapy motivation and family functioning in families with substance abusers. Method: A quasi-experimental research design along with pre-test/post-test and control group was employed for the conduct of this study. The statistical population of this study consisted of all families who presented t...

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Genetic testing and the family.

The family experience of genetic testing is explored in this article. Two family stories are presented to illustrate how families define and manage the ethical and social issues that emerge during 2 types of genetic testing: mutation analysis for Huntington's disease and genetic testing for breast and ovarian cancer susceptibility. These 2 families were purposefully selected because their stori...

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ژورنال

عنوان ژورنال: Psycho-Oncology

سال: 2012

ISSN: 1057-9249

DOI: 10.1002/pon.3139