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6.
Clin Genet ; 56(4): 323-7, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10636452

RESUMO

Herein we discuss Mexican geneticists' views of ethical issues in genetic testing and screening, analyzing whether eugenic principles are involved in this activity. The information was obtained from a comprehensive survey on genetics, ethics, and society organized by Wertz and Fletcher in 1993, in which 37 nations participated. The responses to 21 questions from 64 out of 89 (72%) geneticists invited to participate are analyzed in this paper. The questions were practically the same as those answered recently by a group of Chinese geneticists (Mao X. Chinese geneticists' views of ethical issues in genetic testing and screening: evidence for eugenics in China. Am J Hum Genet 1998: 63: 688-695), who work in a country where the furtherance of eugenic principles is considered to be the goal of human genetics. We concluded that although there are many similarities in the answers from both countries, this is not indicative of Mexican geneticists pursuing eugenic goals because: a) there is no coercion involved; and b) there is no intention of improving the gene pool.


Assuntos
Ética Médica , Eugenia (Ciência) , Testes Genéticos/normas , China , Coleta de Dados , Humanos , México
7.
Am J Hum Biol ; 11(4): 525-529, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-11533972

RESUMO

Several blood groups, ABO, Rh, Ss, Fy, Jk, and red cell acid phosphatase (ACP) types were studied in a native Mixteca population that has resided in Mexico City since 1950. Gene frequencies were obtained and used to establish admixture estimates with blacks and whites. The subjects came from three different geographical areas: High Mixteca, Low Mixteca, and Coast Mixteca. All frequencies were in Hardy-Weinberg equilibrium. The difference in the ABO frequencies was statistically significant when subjects from the three areas were compared simultaneously. Rh frequencies differed only between the High and the Low Mixteca populations. The ACP frequencies were similar between the Low Mixteca population and a previously reported Mestizo population. However, there were significant differences between the High Mixteca group and a Mestizo population, all the subjects being from Oaxaca. This is the first report of Ss, Fy, Jk, and ACP frequencies in a Mixteca population. Am. J. Hum. Biol. 11:525-529, 1999. Copyright 1999 Wiley-Liss, Inc.

8.
Clin Genet ; 54(4): 321-9, 1998 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9831344

RESUMO

Here we discuss the opinion on disclosure issues (respect for confidentiality) of Mexican professionals working in clinical genetics. The information was obtained from a comprehensive survey on genetics, ethics and society organized by Wertz and Fletcher in 1993, in which geneticists from 37 nations participated. The responses to 18 questions from 64 of 89 (72%) geneticists invited to participate were analyzed for this paper. The questions were directed to investigate: a) disclosure of clinically relevant information in several situations such as testicular feminization syndrome, mosaic de novo balanced translocation in a fetus, or accidental discovery of non-paternity; b) the protection of patient's privacy from the spouse or blood relatives; and c) confidentiality in cases with high genetic risk to relatives. The results reveal significant disparity between general responses related to disclosure of all clinically relevant information and specific responses in particular cases. In addition, professionals appear to give higher priority to protecting the spouse, blood relatives or public safety, rather than the patient's confidentiality.


Assuntos
Atitude do Pessoal de Saúde , Confidencialidade , Aconselhamento Genético , Revelação da Verdade , Humanos , México , Inquéritos e Questionários
9.
Am J Med Genet ; 75(4): 426-31, 1998 Feb 03.
Artigo em Inglês | MEDLINE | ID: mdl-9482653

RESUMO

Prenatal diagnosis (PD) provides the physician information on whether the unborn fetus has a genetic or chromosomal disorder, and offers patients a new option: selective abortion. In the present study, we analyzed the answers Mexican geneticists provided to a few selected questions from a multinational survey designed by Wertz and Fletcher [1988: Am J Hum Genet 42:592-600]. The selected questions were related to the use of PD, the acceptance of selective abortion, and the self-reported directiveness of counselling following the diagnosis of a fetal anomaly. Our results show that the great majority of Mexican geneticists participating in the study agree with PD when medically indicated, but not on free demand. Specific cases stimulated the group on thinking more than the general statements provided in the survey. Although the majority agreed that PD should be available to all women, when faced with cases of nonmorbid maternal anxiety, paternity testing, and sex selection, the proportion of geneticists willing to perform the test decreased substantially. When counselling patients on a fetal anomaly, the minority would be as unbiased as possible, and this seems to be the tendency in developing countries where counselling, as stated in the respondents' comments, reflects the belief that the goal of genetics is the prevention of or opposition to abortion. Counselling was influenced by the severity of the disorder. The geneticists' personal attitude toward abortion in the same situations was stronger than when counselling others. Analysis of directiveness in counselling for fetal anomaly showed that older geneticists, with more years of experience in medical genetics, were more likely to be neutral. When counselling directively, the group showed an overall direction toward continuing affected pregnancies. However, older geneticists and those with more than 10 years of practice were more likely than their younger counterparts to counsel towards terminating affected pregnancies. In personal situations of fetal disorder, the general tendency was to abort; however, geneticists seeing more than 5 patients per week, and those who believe that religion is important, were more likely to reject abortion. The sample is representative of Mexican geneticists, and the main limitation of this study is that the geneticists have very little experience in PD, and that their responses were mostly based on theory. However, their opinions may influence the demand and the availability of PD and abortion, as well as the possibility of legalization of abortion on the basis of a fetal defect.


Assuntos
Aborto Induzido/psicologia , Atitude do Pessoal de Saúde , Genética , Diagnóstico Pré-Natal/psicologia , Adulto , Bioética , Feminino , Aconselhamento Genético , Humanos , Masculino , México , Gravidez , Inquéritos e Questionários
10.
Hum Biol ; 69(6): 809-18, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9353976

RESUMO

We describe new information on the frequency and association of class II antigens (HLA-DR and HLA-DQ) of the major histocompatibility complex (MHC) in Mexicans. The study includes HLA-B typing and its association with the HLA-DR antigens determined in 50 families, which included 100 individuals. This family study allowed the establishment of the precise composition of the 200 HLA haplotypes, which cannot be obtained from unrelated individuals. The predominant antigens in decreasing order of frequency were B35, B39, and B61 at the B locus; DR4, DR5, and DR8 at the DR locus; and DQ3 at the DQ locus. The most common HLA-B,HLA-DR haplotype (considering broad specificities) was B16,DR4, with a frequency of 8.0%. Five HLA-B,HLA-DR haplotypes showed significant delta values (observed vs. expected frequencies) after correcting for the number of comparisons. On the other hand, the most common HLA-DR,HLA-DQ haplotypes were DR4,DQ3 and DR5,DQ3 with a frequency higher than 10%. Ten of the 17 HLA-DR,HLA-DQ haplotypes had significant postcorrection delta values.


Assuntos
Etnicidade/genética , Frequência do Gene , Antígenos HLA-B/genética , Antígenos HLA-DQ/genética , Antígenos HLA-DR/genética , Polimorfismo Genético , Variação Genética , Humanos , Índios Norte-Americanos/genética , México , População Branca/genética
11.
Am J Med Genet ; 69(1): 23-8, 1997 Mar 03.
Artigo em Inglês | MEDLINE | ID: mdl-9066879

RESUMO

Most geneticists agree that counselling should be nondirective, and studies report that genetic counselling by geneticists is performed largely in a neutral style. However, couples at risk of having a child with a genetic condition may seek the advice of other physicians. The purpose of the present study was to describe the answers of four groups of specialists from Mexico City (internists, pediatricians, obstetricians, and neurologists) regarding how they would counsel a couple when prenatal diagnosis has shown that a fetus is affected by one of 17 different genetic disorders and to analyze the role of several variables in the development of their opinion. Our results show that physicians in these specialties are more likely to counsel directively than neutrally. Other variables did not influence the directiveness. With respect to direction of influence, internists, pediatricians, and neurologists are more likely to counsel terminating affected pregnancies than are obstetricians (P = 0.0002). Similarly, clinicians older than 37 years of age and those reporting that religion is not important to them counsel terminating affected pregnancies (P = 0.005 and P = 0.003, respectively). Physicians' gender and clinical experience with genetic diseases did not show statistically significant differences. Strong consensus among specialists was reached only on terminating pregnancies in anencephaly. A lowered and moderate consensus (51-75% agreement) was reached on continuing pregnancies with cleft lip and plate. A moderate measure of consensus for nondirective counselling was found among obstetricians regarding 14 of the 17 diseases in the study, whereas neurologists expressed a moderate measure of consensus on counselling the termination of pregnancies when the fetus was affected by neurological disorders. Hence, the approach to counselling was related in part to the fetal condition and in part to the clinician's specialty and age and the self-reported importance of religion. The data presented herein may not be representative of all Mexican physicians within the selected specialties; however, it is important to gather their opinions because they are involved in the care and treatment of genetic diseases and may have an important influence on the demand and availability of prenatal diagnosis and abortion.


Assuntos
Doenças Fetais , Aconselhamento Genético , Medicina , Especialização , Aborto Induzido , Adulto , Tomada de Decisões , Feminino , Humanos , Masculino , México , Gravidez , Probabilidade , Inquéritos e Questionários
12.
Int J Gynaecol Obstet ; 56(1): 47-52, 1997 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9049694

RESUMO

The objective of this study was to analyze physicians' attitudes towards induced abortion with normal fetuses and fetuses known to have an abnormality in various degrees. A total of 193 physicians (internists, pediatricians, gynecologists and neurologists) answered a self-administered questionnaire. The questions were about voluntary abortion; voluntary abortion with malformed fetus; abortion because the fetus has anencephaly; and two questions were asked for the use of prenatal diagnosis and abortion in case of the fetus being the physician's child. The majority of physicians were male, over 35 years, religious and did not have experience with genetic diseases. Few physicians approved abortion of a normal pregnancy, 6 out of 10 agreed if the fetus was malformed, and this number increased to 8 or 9 out of 10 in cases of severe or lethal genetic disease. Gynecologists and neurologists were less in agreement with abortion when pregnancy is normal than the internists and pediatricians (7% vs. 20%). In general the physicians did not have consistent answers. Agreement for abortion was influenced by religious values.


Assuntos
Aborto Induzido , Atitude do Pessoal de Saúde , Médicos , Fatores Etários , Anencefalia , Anormalidades Congênitas , Feminino , Doenças Genéticas Inatas , Humanos , Masculino , México , Gravidez , Religião , Inquéritos e Questionários
14.
Rev Invest Clin ; 48 Suppl: 23-4, 1996 Nov.
Artigo em Espanhol | MEDLINE | ID: mdl-9122544

RESUMO

The published reports on the possibility that the adult type of lactose maldigestion is a hereditary condition are reviewed. The ethnic variability in the frequency of this trait, together with twin and family studies, suggest that this is indeed the case. Family studies, including the one performed in Mexico, indicates that the adult type of lactose maldigestion is inherited in an autosomic recessive manner.


Assuntos
Intolerância à Lactose/genética , Adulto , Humanos
18.
Hum Biol ; 68(3): 395-404, 1996 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8935320

RESUMO

We analyze the possible effect of gene flow on the genetic structure of present-day Mexicans. For this purpose we reviewed previous admixture estimates for various Indian and Mestizo groups. Several facts seem clear: (1) There are no pure Indian groups in Mexico, because all Indian groups show variable degrees of admixture, mostly with whites (range, 0.088 in the Huichol to 0.373 in the Huasteco); (2) the main ancestral contribution to the noncoastal lower middle class Mestizo populations is Indian (above 50%) so that from a genetic standpoint Indians and lower middle class Mestizos are not much different; and (3) black ancestry is quite high on the coasts, ranging from 0.127 to 0.405 on the east coast, and is present in other Mestizos, ranging in large urban centers from 0.027 in Oaxaca to 0.107 in Puebla and in smaller cities from 0.08 in Tlaxcala to 0.181 in Cuanalán.


Assuntos
Etnicidade/genética , Índios Norte-Americanos/genética , População , População Branca/genética , Emigração e Imigração , Humanos , México
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