Making Sense of New Disease Categories
Naming, Spatialising, and Serialising in Genomic Medicine
Bibliographic Data
| ID | 3665481 |
|---|---|
| Authors | Laura E Navne (0000-0001-8996-3222, VIVE - The Danish Center for Social Science Research, corresponding author) |
| Year | 2023 |
| Volume | 10 |
| Issue | 3 |
| Pages | 1-28 |
| Publication date | 2023-09-27 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Medicine Anthropology Theory (JOURNAL) |
| Journal identifiers | ISSN: 2405-691X • E-ISSN: 2405-691X |
| Publisher | Edinburgh University Library (PUBLISHER) |
| DOI | 10.17157/mat.10.3.6686 |
| OpenAlex | W4387364367 |
| Language | EN |
| Citations received | 4 |
| References cited | 35 |
Intrigued by geneticists' framing of new gene names as somehow devoid of meaning, I set out to explore how patients and families make sense of naming practices in the field of genomic medicine. The aim for ever-more precise disease categorisation has resulted in names for medical conditions that are more akin to car-licence plates, such as DPF2 and G246A. Conducting fieldwork in Denmark, I followed the introduction of personalised medicine-that is the aim to tailor prevention, diagnosis, and treatment to the individual based on genomic and other data-in the field of rare diseases and diabetes. Engaging with theories of naming, spatialisation and serialisation, I suggest that it is exactly because of their unsettled meaning and presupposed lack of history that new gene names provide patients extra room for creative identity work. I argue that some patients and families use the new genetic disease labels to escape unwanted moral regimes, relocating disease aetiology from a moralised landscape to a 'molecularised' genetic one. I discuss how practices of serialisation enable patients to feel recognised as unique persons. In conclusion, I suggest that while the new genetic names may not stigmatise, they do change the patients' idea of who they are in surprising ways, some of which the geneticists had not anticipated
Disease · Epistemology · Pathology · Psychotherapist · Biomedical Ethics and Regulation · BRCA gene mutations in cancer · Genomics and Rare Diseases · History · Medicine · Philosophy · Psychology
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Contested futures
Strategies of stratification
The birth of the clinic
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Discipline and Punish
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Digital phenotyping and data inheritance
Genomics and the Reimagining of Personalized Medicine
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Visualising difference, similarity and belonging in paediatric genetics
De novo kin
Expansion and uncertainty
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Looping Genomes
Comprehending the Body in the Era of the Epigenome
For a Sociology of Expertise
Genomics as public health? Community genetics and the challenge of personalised medicine in Cuba
Eugenics, Epigenetics, and Obesity Predisposition among Mexican Mestizos
Careography
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| Unique citing works | 4 |
|---|---|
| Citations per year | 2 |
| Citation span | 2024 - 2025 (2) |
| Citation velocity | recent |
| Highly cited | No |
| Citation types | Neutral: 4 |