RESUMEN
This article considers the existential and eugenic risks of gene editing with CRISPR-Cas9. It brings forward epistemological and phenomenological questions concerning what CRISPR technology suggests about the limits of being human. By illuminating the paradoxical relationship between our "then self" and "now self," it considers the fragility of our individual and collective future-making endeavors. To do this, the article offers an overview of the existential dilemmas facing modern subjects, a history of eugenics and the ideology of health, a meditation on the limits of human knowledge, and an explication of the cultural work of metaphor. It argues for the benefits of human variation for individuals and communities and concludes by calling for an attitude of humility and restraint to guide the development and implementation of humane technologies rather than genetic manipulation technologies that aim to control future outcomes through present actions.
Asunto(s)
Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Espaciadas , Ética Médica , Eugenesia/métodos , Edición Génica/ética , Técnicas Reproductivas Asistidas/ética , Trastorno Autístico , Niño , Niños con Discapacidad , Femenino , Humanos , Conocimiento , Padres , EmbarazoRESUMEN
BACKGROUND: The founders of Hereditas envisioned that race biology would be a major subject that had social applications with utmost importance in the near future. Anthropometrics was in this context understood to be the pure and eugenics the applied science. Sweden had a long tradition in physical anthropometry. Herman Lundborg, member of the advisory board of Hereditas, united the anthropometric and eugenic approaches in a synthesis. He was the first head of the Institute for Race Biology in Sweden. The contents of Hereditas reflect the development of race biology in the Nordic countries. CONCLUSIONS: The initial enthusiasm for applied race biology did not last long. In the 1920's Hereditas carried papers on both physical anthropology and eugenics. Most paper dealt, however, with human genetics without eugenic content. Two papers, published in 1921 and 1939 show how the intellectual climate had changed from positive to negative. Finally only human genetics prevailed as the legitimate study of the human race or humankind. A belated defense of eugenics published in 1951 did not help; geneticists had abandoned anthropometrics for good around the year 1940 and eugenics about a decade later. In spite of that, eugenic legislation was amended astonishingly late, in the 1970's. The development was essentially similar in all Nordic countries.
Asunto(s)
Biología , Eugenesia , Antropometría/métodos , Biología/historia , Biología/métodos , Biología/tendencias , Cruzamiento , Eugenesia/historia , Eugenesia/métodos , Eugenesia/tendencias , Estudios de Asociación Genética , Genética de Población , Historia del Siglo XX , Genética Humana , Humanos , Fitomejoramiento , Grupos Raciales/genética , Países Escandinavos y NórdicosRESUMEN
This essay explores how hormone treatments were used to optimize and normalize individuals under Italian Fascism. It does so by taking the activities of the Biotypological Orthogenetic Institute - an Italian eugenics and endocrinological centre founded by Nicola Pende in 1926 - as the prime example of a version of eugenics, biotypology, which was based on hormone therapies. This essay first demonstrates that Italian Fascist biopolitics was not only concerned with increasing the size of the Italian population, but also with improving its quality. It suggests that under the Italian Fascist regime hormone therapies became eugenic tools of intervention to improve the Italian race. Second, while Pende's institute purportedly enhanced men and women, its activities show the extent to which the 'techniques of normalization' pursued by the Fascist regime were both systematic and invasive.
Asunto(s)
Eugenesia/historia , Fascismo/historia , Terapia de Reemplazo de Hormonas/historia , Anatomía/clasificación , Anatomía/historia , Eugenesia/métodos , Femenino , Historia del Siglo XX , Cuerpo Humano , Humanos , Italia , Masculino , Valores de ReferenciaRESUMEN
This article deals with the nine European nations which legalised non-consensual sterilisation during the interwar years, thus completing the review, the first part of which was published in an earlier issue of this Journal. Like we did for North America, Japan and Mexico, countries concerned are addressed in chronological order, as practices in one of these influenced policies in others, involved later. For each, we assess the continuum of events up to the present time. The Swiss canton of Vaud was the first political entity in Europe to introduce a law on compulsory sterilisation of people with intellectual disability, in 1928. Vaud's sterilisation Act aimed at safeguarding against the abusive performance of these procedures. The purpose of the laws enforced later in eight other European countries (all five Nordic countries; Germany and, after its annexation by the latter, Austria; Estonia) was, on the contrary, to effect the sterilisation of large numbers of people considered a burden to society. Between 1933 and 1939, from 360,000 [corrected] to 400,000 residents (two-thirds of whom were women) were compulsorily sterilised in Nazi Germany. In Sweden, some 32,000 sterilisations carried out between 1935 and 1975 were involuntary. It might have been expected that after the Second World War ended and Nazi legislation was suspended in Germany and Austria, including that regulating coerced sterilisation, these inhuman practices would have been discontinued in all nations concerned; but this happened only decades later. More time still went by before the authorities in certain countries officially acknowledged the human rights violations committed, issued apologies and developed reparation schemes for the victims' benefit.
Asunto(s)
Eugenesia/historia , Eugenesia/métodos , Esterilización Involuntaria/historia , Esterilización Involuntaria/legislación & jurisprudencia , Compensación y Reparación/historia , Compensación y Reparación/legislación & jurisprudencia , Europa (Continente) , Eutanasia/historia , Eutanasia/legislación & jurisprudencia , Historia del Siglo XX , Humanos , Discapacidad IntelectualRESUMEN
This article applies tools from argumentation theory to slippery slope arguments used in current ethical debates on genetic engineering. Among the tools used are argumentation schemes, value-based argumentation, critical questions, and burden of proof. It is argued that so-called drivers such as social acceptance and rapid technological development are also important factors that need to be taken into account alongside the argumentation scheme. It is shown that the slippery slope argument is basically a reasonable (but defeasible) form of argument, but is often flawed when used in ethical debates because of failures to meet the requirements of its scheme.
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Disentimientos y Disputas , Eugenesia/métodos , Ingeniería Genética/ética , Argumento Refutable , Humanos , Invenciones , Principios Morales , Justicia Social , Valores SocialesRESUMEN
Genomic medicine offers a growing number of methods to diagnose, cure or prevent disability. Although many disabled people welcome these advances, others have reservations about the impact of genetic knowledge on disabled people's lives, arguing that genetic science might exacerbate the deep ambivalence that society as a whole has towards physical difference and anomaly. It is also possible, however, that being able to specify the genetic bases of disability, and distinguish them from other causative factors, will contribute to a fuller understanding of disability and a better response to disabled people.
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Personas con Discapacidad/psicología , Enfermedades Genéticas Congénitas/diagnóstico , Enfermedades Genéticas Congénitas/genética , Medicina/tendencias , Diagnóstico Prenatal/psicología , Eugenesia/métodos , Eugenesia/tendencias , Enfermedades Genéticas Congénitas/psicología , Genética Médica/ética , Genética Médica/tendencias , Genoma Humano , Conocimientos, Actitudes y Práctica en Salud , Humanos , Técnicas de Diagnóstico Molecular/tendencias , PrejuicioAsunto(s)
Protección a la Infancia/historia , Eugenesia/historia , Eugenesia/métodos , Pobreza/estadística & datos numéricos , Esterilización Involuntaria/historia , Esterilización Involuntaria/métodos , Esterilización Reproductiva/historia , Adulto , Niño , Preescolar , Femenino , Historia del Siglo XX , Humanos , Lactante , Recién Nacido , Masculino , Estados UnidosRESUMEN
The Halifax Explosion provided the opportunity for an "experiment in public health" that was meant not only to restore but also to improve the city and its population in the process. The restructuring that occurred during the restoration was influenced by pre-existing ideals and prejudices which were reflected in the goals of the newly formed committees in charge of the reconstruction. The primary emphasis on improvement as well as control was the result of existing regional concerns regarding the emigration of the province's most "desirable" stock, in the form of healthy, educated young men and women, to central Canada and the eastern United States. Public health reforms reflected the eugenic goal of improving the overall quality of the population through education, surveillance, and inspection, resorting finally to institutionalizing people who public health officials determined were genuinely deficient.
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Eugenesia/historia , Reforma de la Atención de Salud/historia , Salud Pública/historia , Desastres/historia , Eugenesia/legislación & jurisprudencia , Eugenesia/métodos , Historia del Siglo XX , Migración Humana/historia , Humanos , Institucionalización/historia , Nueva Escocia , Salud Pública/legislación & jurisprudencia , Salud Pública/métodosRESUMEN
Prejudice and stigma against people with mental illness can be seen throughout history. The worst instance of this prejudice was connected to the rise of the eugenics movement in the early 20th century. Although the Nazi German T-4 program of killing people with mental illness was the most egregious culmination of this philosophy, the United States has its own dark eugenics history-nearing a slippery slope all too similar to that of the Nazis. Mental health care clinicians need to examine this period to honor the memory of the victims of eugenics and to guarantee that nothing like this will ever happen again.
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Eugenesia/historia , Trastornos Mentales/historia , Nacionalsocialismo/historia , Prejuicio/historia , Índice de Severidad de la Enfermedad , Eugenesia/métodos , Alemania/epidemiología , Historia del Siglo XX , Humanos , Trastornos Mentales/epidemiología , Prejuicio/psicología , Estados Unidos/epidemiologíaRESUMEN
John Harris and Julian Savulescu, leading figures in the "new' eugenics, argue that parents are morally obligated to use genetic and other technologies to enhance their children. But the argument they give leads to conclusions even more radical than they acknowledge. Ultimately, the world it would lead to is not all that different from that championed by eugenicists one hundred years ago.
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Discusiones Bioéticas , Eugenesia/tendencias , Fertilización In Vitro/ética , Mejoramiento Genético/ética , Obligaciones Morales , Eugenesia/métodos , Fertilización In Vitro/tendencias , Predicción , Mejoramiento Genético/normas , Humanos , Técnicas de Transferencia Nuclear/ética , Técnicas de Transferencia Nuclear/normas , Diagnóstico Preimplantación/ética , Diagnóstico Preimplantación/métodosRESUMEN
The CRISPR editing method is revolutionary. This technique opens the possibility of countless operations in the genome of living beings. However, the risks are high and, in some cases, unpredictable. Therefore, based on an anthropology that recognizes the human person with an inherent dignity that includes the body, this article intends to propose bases for a regulation capable of facing the challenge of CRISPR, especially, given the possibility of confusing its therapeutic resource with the eugenics, also before the imminent risk of unleashing unforeseen consequences such as mutations, malformations and side effects that could be devastating for human life.
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Sistemas CRISPR-Cas , Mejoramiento Genético/ética , Comunicación Interdisciplinaria , Antropología , Biotecnología/ética , Biotecnología/legislación & jurisprudencia , Biotecnología/métodos , Anomalías Congénitas/genética , Eugenesia/legislación & jurisprudencia , Eugenesia/métodos , Edición Génica , Mejoramiento Genético/legislación & jurisprudencia , Mejoramiento Genético/métodos , Terapia Genética , Genoma Humano , Características Humanas , Derechos Humanos , Humanos , Internacionalidad , Mutación , Filosofía , RespetoAsunto(s)
Eugenesia/historia , Holocausto/historia , Rol del Médico/historia , Mala Conducta Científica/ética , Mala Conducta Científica/historia , Eugenesia/métodos , Alemania , Historia del Siglo XX , Historia del Siglo XXI , Holocausto/ética , Humanos , Principios Morales , Estados Unidos , Crímenes de Guerra/ética , Crímenes de Guerra/historiaRESUMEN
The article below is intended to reflect on whether or not a eugenic tendency constitutes an intrinsic element of human fertilization in vitro. The author outlines ideas and circumstances which characterized the foundation and propagation of eugenics between the eighteenth and nineteenth centuries. A brief discussion follows on some of the standard procedures of in vitro fertilization, and in particular, those which manifest a trace or hint of eugenics--heterologous fertilization and sperm banking, preimplantation genetic diagnosis (PGD) and embryo selection--practices which, nonetheless, are used on a large scale and shed light on both the essence of procreative medicine and on the current cultural environment. The objective of the article is to explore whether it is possible to eliminate the eugenic connotations without foregoing the benefits of technical and scientific progress.
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Eugenesia , Genética/ética , Técnicas Reproductivas Asistidas/ética , Eugenesia/historia , Eugenesia/métodos , Eugenesia/tendencias , Europa (Continente) , Femenino , Historia del Siglo XIX , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Masculino , Diagnóstico Preimplantación/ética , Preselección del Sexo/ética , Estados UnidosRESUMEN
Criminal behaviour is but one behavioural tendency for which a genetic influence has been suggested. Whilst this research certainly raises difficult ethical questions and is subject to scientific criticism, one recent research project suggests that for some families, criminal tendency might be predicted by genetics. In this paper, supposing this research is valid, we consider whether intervening in the criminal tendency of future children is ethically justifiable. We argue that, if avoidance of harm is a paramount consideration, such an intervention is acceptable when genetic selection is employed instead of genetic enhancement. Moreover, other moral problems in avoiding having children with a tendency to criminal behaviour, such as the prospect of social discrimination, can also be overcome.
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Crimen , Análisis Ético , Eugenesia , Genética Conductual , Diagnóstico Preimplantación/ética , Violencia , Trastorno de Personalidad Antisocial/genética , Investigación Conductal/ética , Niño , Conducta de Elección , Cromosomas Humanos X , Crimen/prevención & control , Transferencia de Embrión , Eugenesia/métodos , Femenino , Fertilización In Vitro , Determinismo Genético , Mejoramiento Genético/ética , Predisposición Genética a la Enfermedad , Investigación Genética/ética , Pruebas Genéticas/ética , Humanos , Masculino , Monoaminooxidasa/genética , Padres , Paternalismo/ética , Prejuicio , Diagnóstico Prenatal/ética , Preselección del Sexo/ética , Violencia/prevención & control , Derecho de no NacerAsunto(s)
Eugenesia/métodos , Edición Génica/ética , Reproducción/genética , Justicia Social/ética , Poblaciones Vulnerables , Aborto Inducido/ética , Sistemas CRISPR-Cas/genética , Eugenesia/historia , Femenino , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Participación del Paciente , Esterilización Involuntaria/ética , Esterilización Involuntaria/historia , Confianza , Estados UnidosRESUMEN
This paper discusses and analyses three articles appearing in a 1942 issue of the American Journal of Psychiatry. In the first, neurologist Foster Kennedy argued that 'feebleminded' people should be killed (an act which he referred to as 'euthanasia'). The rebuttal was written by psychiatrist Leo Kanner, who argued against 'euthanasia'. An unsigned editorial discussing these positions clearly sided with Kennedy: that 'euthanasia' would be appropriate in some cases, and that parents' opposition to this procedure should be the subject of psychiatric concern. The arguments are analysed and discussed within the context of eugenics and the murder of mental patients in Germany. Finally, the author points out that currently ascendant genetic theories in psychiatry could be a precursor for future proposals similar to Kennedy's.
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Eugenesia/historia , Eutanasia Activa/historia , Discapacidad Intelectual/historia , Psiquiatría/historia , Adulto , Niño , Eugenesia/métodos , Historia del Siglo XX , Humanos , Padres/psicología , Publicaciones Periódicas como Asunto/historia , Estados UnidosRESUMEN
Because genes and alterations within them determine the identity, characteristics, and inheritance of every individual, the application of genetic science to humans has long been surrounded by apprehension, controversy, and real or perceived potential for abuse. Crude eugenics practices of the past now find a theoretical rebirth and transformation through the use of modern molecular genetic technologies for mutation detection, predictive and prenatal diagnosis, and, ultimately, gene replacement. The advent of oligonucleotide microarray analysis, in which hundreds or thousands of genes and mutations can be tested in parallel, offers tremendous promise for more accurate, sensitive, and efficient genetic testing. At the same time, however, this powerful technology dramatically increases the number and scope of ethical concerns accompanying each individual test request. This article considers the evolution and implications of these concerns, from the initial ordering of a microarray test by the physician to such issues as informed consent, privacy, confidentiality, clinical utility, discrimination, stigmatization, ethnic and population impact, and reimbursement.