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1.
Rev Cient Odontol (Lima) ; 10(4): e133, 2023.
Artigo em Espanhol | MEDLINE | ID: mdl-38390609

RESUMO

Bad habits, such as poor posture during the use of technological devices, poor abdominal control and oral breathing pattern can lead to a forward head position, which has important implications for the entire future of the individual, especially at the stomatognathic system. There is a strong association between temporomandibular disorders and forward head syndrome. Where the muscular component is the main affected, with the appearance of more trigger points at the level of the sternocleidomastoid muscles, upper trapezius, rectus capitis posterior and upper oblique capitis. Degenerative changes in the temporomandibular joint have been observed, but evidence is still lacking to ensure that Forward Head Syndrome is the etiological factor.

2.
Hum Immunol ; 81(9): 461-474, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32651014

RESUMO

We studied HLA class I (HLA-A, -B) and class II (HLA-DRB1, -DQB1) allele groups and alleles by PCR-SSP based typing in a total of 15,318 mixed ancestry Mexicans from all the states of the country divided into 78 sample sets, providing information regarding allelic and haplotypic frequencies and their linkage disequilibrium, as well as admixture estimates and genetic substructure. We identified the presence of 4268 unique HLA extended haplotypes across Mexico and find that the ten most frequent (HF > 1%) HLA haplotypes with significant linkage disequilibrium (Δ'≥0.1) in Mexico (accounting for 20% of the haplotypic diversity of the country) are of primarily Native American ancestry (A*02~B*39~DRB1*04~DQB1*03:02, A*02~B*35~DRB1*08~DQB1*04, A*68~B*39~DRB1*04~DQB1*03:02, A*02~B*35~DRB1*04~DQB1*03:02, A*24~B*39~DRB1*14~DQB1*03:01, A*24~B*35~DRB1*04~DQB1*03:02, A*24~B*39~DRB1*04~DQB1*03:02, A*02~B*40:02~DRB1*04~DQB1*03:02, A*68~B*35~DRB1*04~DQB1*03:02, A*02~B*15:01~DRB1*04~DQB1*03:02). Admixture estimates obtained by a maximum likelihood method using HLA-A/-B/-DRB1 as genetic estimators revealed that the main genetic components in Mexico as a whole are Native American (ranging from 37.8% in the northern part of the country to 81.5% in the southeastern region) and European (ranging from 11.5% in the southeast to 62.6% in northern Mexico). African admixture ranged from 0.0 to 12.7% not following any specific pattern. We were able to detect three major immunogenetic clusters correlating with genetic diversity and differential admixture within Mexico: North, Central and Southeast, which is in accordance with previous reports using genome-wide data. Our findings provide insights into the population immunogenetic substructure of the whole country and add to the knowledge of mixed ancestry Latin American population genetics, important for disease association studies, detection of demographic signatures on population variation and improved allocation of public health resources.


Assuntos
Alelos , Genética Populacional/métodos , Antígenos HLA/genética , Complexo Principal de Histocompatibilidade/genética , Polimorfismo de Nucleotídeo Único , DNA/genética , DNA/isolamento & purificação , Frequência do Gene , Genoma Humano , Haplótipos , Humanos , Desequilíbrio de Ligação , México
3.
Curr Biol ; 30(11): 2078-2091.e11, 2020 06 08.
Artigo em Inglês | MEDLINE | ID: mdl-32359431

RESUMO

The forced relocation of several thousand Africans during Mexico's historic period has so far been documented mostly through archival sources, which provide only sparse detail on their origins and lived experience. Here, we employ a bioarchaeological approach to explore the life history of three 16th century Africans from a mass burial at the San José de los Naturales Royal Hospital in Mexico City. Our approach draws together ancient genomic data, osteological analysis, strontium isotope data from tooth enamel, δ13C and δ15N isotope data from dentine, and ethnohistorical information to reveal unprecedented detail on their origins and health. Analyses of skeletal features, radiogenic isotopes, and genetic data from uniparental, genome-wide, and human leukocyte antigen (HLA) markers are consistent with a Sub-Saharan African origin for all three individuals. Complete genomes of Treponema pallidum sub. pertenue (causative agent of yaws) and hepatitis B virus (HBV) recovered from these individuals provide insight into their health as related to infectious disease. Phylogenetic analysis of both pathogens reveals their close relationship to strains circulating in current West African populations, lending support to their origins in this region. The further relationship between the treponemal genome retrieved and a treponemal genome previously typed in an individual from Colonial Mexico highlights the role of the transatlantic slave trade in the introduction and dissemination of pathogens into the New World. Putting together all lines of evidence, we were able to create a biological portrait of three individuals whose life stories have long been silenced by disreputable historical events.


Assuntos
DNA Antigo/análise , Pessoas Escravizadas/história , Nível de Saúde , Hepatite B/história , Bouba/história , Adulto , Arqueologia , População Negra/história , Vírus da Hepatite B/isolamento & purificação , História do Século XVI , Humanos , Masculino , México , Treponema/isolamento & purificação , Adulto Jovem
4.
Recurso educacional aberto em Português | CVSP - Brasil | ID: una-5812

RESUMO

O aleitamento materno é a mais sábia estratégia natural de vínculo, afeto, proteção e nutrição para a criança. Sendo assim, o incentivo ao aleitamento materno exclusivo até os seis meses de idade é uma importante ação de promoção da saúde e de prevenção de agravos. Contudo, a realidade vivenciada pela autora aponta para uma prática de abandono precoce do aleitamento materno, cada vez mais adotada pelas mães colocando em risco o desenvolvimento das crianças. Diante deste contexto, o presente estudo propôs demonstrar com base na revisão da literatura que as ações desenvolvidas pelo Programa Saúde da Família podem reduzir os índices de abandono precoce do aleitamento materno exclusivo. A revisão bibliográfica baseou-se em artigos científicos das Bases de Dados SciELo, LILACS, OMS, dentre outros. As informações foram pesquisadas num período aproximado de 82 dias, de 26 de junho a 15 de setembro de 2011. O tema abordado foi o Programa Saúde da Família e as intervenções voltadas para a prática do aleitamento materno exclusivo. Faz-se necessária a detecção de forma precoce dos fatores que causam o desmame, para que com isso se torne possível o direcionamento e a organização das ações desenvolvidas pelos profissionais da equipe de saúde da família, buscando criar alternativas para melhorar a assistência ao binômio mãe/ filho prolongando o período do aleitamento materno exclusivo.


Assuntos
Desmame , Estratégias de Saúde Nacionais , Aleitamento Materno
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