Hereditary cancer syndromes

27Citations
Citations of this article
76Readers
Mendeley users who have this article in their library.

Abstract

Objective. - To summarize the biological basis, clinical implications, identification, and medical management of syndromes associated with increased risk of common adult cancers. Data Sources. - Recent studies and data available from molecular and clinical analysis of genes responsible for autosomal-dominant inheritance of cancer risk. Data Synthesis. - Several hereditary cancer syndromes have been identified for which there are increasingly effective diagnostic and management options. Specific hereditary susceptibility syndromes have been characterized that increase the risk of malignancies of the breast, ovary, colon, endometrium, and endocrine organs. Following a summary of the biological basis of hereditary cancer risk in adults, the identification of such syndromes by clinical and laboratory means is reviewed. Finally, management options for individuals with these syndromes are summarized. Conclusions. - Advances in gene discovery have allowed the diagnosis of recently characterized hereditary cancer syndromes to enhance medical management for individuals with inherited susceptibility to common cancers.

Cite

CITATION STYLE

APA

Frank, T. S. (2001). Hereditary cancer syndromes. Archives of Pathology and Laboratory Medicine, 125(1), 85–90. https://doi.org/10.5858/2001-125-0085-hcs

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free