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1.
Braz. j. morphol. sci ; 30(2): 115-120, 2013. ilus, tab
Artigo em Inglês | LILACS | ID: lil-699339

RESUMO

Introduction: The purpose of this paper is to determine the topography, biometry and light microscopyimage of the vesicular and bulbourethral glands in order to analyze morphologic features of the accessorysexual glands in castrated and non-castrated animals.Materials and Methods:The morphology of theaccessory sexual glands was investigated in 14 adult Santa Inesbreed sheep, weighing 32 kg, on average.Six of them were castrated, and eight, non-castrated. For macroscopic study, the description of these twoglands was carried out, as well as dissection and biometry study. Moreover, weight, length, height andwidth measurements were evaluated. For histological analysis, the vesicular and bulbourethral glands weresampled.Results:The topography of the reproductive glands was similar to bovine species. However, lowermacroscopic measurements (p < 0,05) in the glands of the castrated sheep were evidenced when comparedwith the non-castrated ones. Characteristics such as shape of the glands, composition of the layer mucosa,the lamina propria, muscular, the excretory ducts and the adventitia were determined.Conclusion:Sheepcastration promoted changes in the biometric measures of the glands, which were lower in castrated animals.The morphological and biometric characteristics of the vesicular and bulbourethral glands in sheep weredetermined.


Assuntos
Animais , Masculino , Biometria , Glândulas Bulbouretrais/anatomia & histologia , Glândulas Bulbouretrais/ultraestrutura , Glândulas Seminais/anatomia & histologia , Glândulas Seminais/ultraestrutura , Histologia , Ovinos/anatomia & histologia , Castração/efeitos adversos , Dissecação , Interpretação Estatística de Dados
2.
Indian J Dent Res ; 23(5): 585-90, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23422601

RESUMO

OBJECTIVE: The purpose of the present study was to assess the knowledge regarding emergency management of tooth avulsion among elementary schoolteachers in the city of Jaboatão dos Guararapes, Pernambuco, Brazil. MATERIALS AND METHODS: A total of 338 teachers answered a questionnaire with items on emergency procedures following tooth avulsion. RESULTS: The majority of teachers (89.1%) had received no previous orientation regarding management of dental trauma and 81.4% had not witnessed an accident in which tooth avulsion had occurred. If an avulsed tooth had fallen to the ground, 84.3% of the teachers said they would pick it up, and 67.8% of them stated that they would clean it with water or some other liquid. A total of 33.1% said that they would take the student with the tooth in hand to a dental office. Of the respondents 88.5% would seek professional help immediately; 85.2% stated they would be unable to reimplant the avulsed tooth; and 39.3% would store the tooth in water. CONCLUSIONS: A lack of technical information was observed among teachers regarding management of tooth avulsion. Educational campaigns at schools are necessary to modify the behavior of the teachers with regard to management of tooth avulsion. Further studies should be carried out for the assessment of teachers who have participated in educational campaigns to make the treatment of dental trauma a matter of public interest.


Assuntos
Tratamento de Emergência , Docentes , Conhecimentos, Atitudes e Prática em Saúde , Avulsão Dentária/terapia , Acidentes , Adolescente , Adulto , Atitude Frente a Saúde , Brasil , Criança , Pré-Escolar , Assistência Odontológica , Feminino , Educação em Saúde Bucal , Humanos , Masculino , Soluções para Preservação de Órgãos/uso terapêutico , Inquéritos e Questionários , Reimplante Dentário , Água
3.
Genet Couns ; 15(3): 303-10, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15517822

RESUMO

Complex chromosome rearrangements (CCR) involving multiple breaks in two or more chromosomes are rare. We describe a girl with development delay and overgrowth who presents a nine-break apparently balanced de novo rearrangement involving chromosomes 1, 2, 3, 4 and 12, and a boy with developmental delay and seizures with a complex three-chromosome apparently balanced de novo rearrangement involving chromosomes 2, 7 and 13. The relationship between clinical abnormalities and apparently balanced rearrangements is discussed.


Assuntos
Aberrações Cromossômicas , Transtornos Cromossômicos/genética , Translocação Genética , Adolescente , Bandeamento Cromossômico , Transtornos Cromossômicos/diagnóstico , Cromossomos Humanos Par 1/genética , Cromossomos Humanos Par 12/genética , Cromossomos Humanos Par 13/genética , Cromossomos Humanos Par 2/genética , Cromossomos Humanos Par 3/genética , Cromossomos Humanos Par 4/genética , Cromossomos Humanos Par 7/genética , Feminino , Humanos , Hibridização in Situ Fluorescente/métodos , Deficiência Intelectual/diagnóstico , Deficiência Intelectual/genética , Masculino , Microcefalia/complicações , Hipotonia Muscular/complicações
4.
Am J Med Genet ; 94(4): 281-3, 2000 Oct 02.
Artigo em Inglês | MEDLINE | ID: mdl-11038439

RESUMO

Ablepharon-macrostomia syndrome (AMS) is a rare condition comprising severe deficiency of the anterior lamella of both eyelids, abnormal ears, macrostomia, anomalous genitalia, redundant skin, and absence of lanugo. There is no agreement about cause; some authors suggest autosomal recessive inheritance. We describe familial occurrence of AMS in a girl, sister of a previously reported patient. The father has facial anomalies that suggest autosomal dominant inheritance. Am. J. Med. Genet. 94:281-283, 2000.


Assuntos
Anormalidades Múltiplas/genética , Pálpebras/anormalidades , Transtornos do Crescimento/genética , Macrostomia/genética , Adulto , Pré-Escolar , Pálpebras/crescimento & desenvolvimento , Feminino , Genes Dominantes , Genitália Feminina/anormalidades , Genitália Feminina/crescimento & desenvolvimento , Transtornos do Crescimento/diagnóstico , Cabelo/anormalidades , Cabelo/crescimento & desenvolvimento , Humanos , Lactente , Recém-Nascido , Masculino , Núcleo Familiar , Gravidez , Síndrome
5.
Clin Dysmorphol ; 8(4): 301-3, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10532183

RESUMO

A new case of Hernandez syndrome is described in a 16-year-old Brazilian girl. The syndrome consists mainly of psychomotor retardation, epilepsy, a bulbous nose and obesity.


Assuntos
Deficiências do Desenvolvimento , Epilepsia , Nariz/anormalidades , Desempenho Psicomotor , Adolescente , Feminino , Humanos , Obesidade , Síndrome
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