Format

Send to

Choose Destination
See comment in PubMed Commons below
Endeavour. 2012 Jun;36(2):77-84. doi: 10.1016/j.endeavour.2011.12.002. Epub 2012 Jan 16.

Visualizing carrier status: fragile X syndrome and genetic diagnosis since the 1940s.

Author information

1
University of Pennsylvania, History and Sociology of Science, 303 Claudia Cohen Hall, Philadelphia, PA 19104, United States. ahog@sas.upenn.edu

Abstract

What does it look like to be the carrier of a genetic disease? Carrier status may be determined through the visual analysis of both genotypic and phenotypic evidence. Over the past 70 years, clinical geneticists have depended upon multiple strategies for identifying disease carriers within a family. This has included pedigree analysis, which was based upon clinical observations of individual family members and, in recent decades, cytogenetic and molecular methods. Newer techniques have offered novel opportunities to actually see the suspected etiological markers of certain genetic diseases, such as Fragile X syndrome. The visualization of these markers has both clarified and confused previously observed inheritance patterns, in some cases leading to the development of newly distinct diagnostic categories. As a result, what it means to be affected by, or the carrier of, a genetic disease has continuously evolved.

PMID:
22257912
DOI:
10.1016/j.endeavour.2011.12.002
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Elsevier Science
    Loading ...
    Support Center