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2.
Gac Med Mex ; 136(6): 585-94, 2000.
Artigo em Espanhol | MEDLINE | ID: mdl-11131860

RESUMO

One of the great challenges in molecular biology is to understand the mechanisms by which a particular genetic defect gives origin to a specific disease. Mitochondrial DNA is more susceptible than nuclear DNA to mutations. Mitochondrial mutations have been associated with a wide spectrum of disorders characterized by a complex phenotype and actually named mitochondrial cytopathies or oxidative phosphorylation diseases. The objective of this paper is to review the relevant genetic, clinical, and morphologic features of cardiac involvement in this heterogeneous but exciting group of diseases. The clinical features of cardiac involvement in mitochondrial cytopathies vary in the different subgroups of these disorders and in particular, mitochondrial mutations can causes characteristic cardiac abnormalities.


Assuntos
DNA Mitocondrial/genética , Miopatias Mitocondriais/genética , DNA Mitocondrial/fisiologia , Cardiopatias/genética , Humanos , Miopatias Mitocondriais/patologia , Mutação , Oxirredução , Fosforilação Oxidativa , Fenótipo
3.
Gac Med Mex ; 136(2): 159-62, 2000.
Artigo em Espanhol | MEDLINE | ID: mdl-10815326

RESUMO

Forty years have gone by since the first pacemaker implant; this fact had strong impact in the life of thousands of persons. The objective of this work is to report the case of definitive pacemaker malfunction with epicardiac lead and review the literature concerning the important aspects of the causes and diagnosis of pacemaker malfunction. We consider that physicians dealing with patients implanted these devices must be prepared to diagnose and treat them adequately.


Assuntos
Marca-Passo Artificial/efeitos adversos , Síndrome de Adams-Stokes/diagnóstico , Síndrome de Adams-Stokes/terapia , Idoso , Eletrocardiografia , Eletrodos/efeitos adversos , Falha de Equipamento , Feminino , Bloqueio Cardíaco/diagnóstico , Bloqueio Cardíaco/terapia , Humanos , Retratamento
4.
Gac Med Mex ; 135(6): 641-51, 1999.
Artigo em Espanhol | MEDLINE | ID: mdl-10605266

RESUMO

The heart and blood have inspired the interest of many cultures'. Even before the heart became a subject of scientific study it was considered as a host to deities and feelings. Prehispanic peoples who inhabited Mesoamerica were not the exception. The heart and blood became the core of the life force and the link to a religious doctrine. It is very clear that these people knew the anatomy of the heart for their human sacrifices to their gods, to maintain the steady course of the planets through out the universe, which consisted of skillfully removing this vital organ as well as the blood for their offerings. Works of art such as paintings, sculptures, carvings, ceramics and even poetry portray the importance of the heart and blood in culture and religion. The aim of this review is to study from the historical and medical point of view, the heart and blood, and their importance to the early Mexicans, to enable them to face and understand the world around them.


Assuntos
Arte/história , Sangue , Cardiologia/história , Coração , Medicina Tradicional/história , Mitologia , Religião/história , Sociedades Médicas/história , Adulto , Criança , História do Século XVII , História do Século XVIII , História do Século XX , História Antiga , Humanos , México
5.
Rev Invest Clin ; 51(2): 121-34, 1999.
Artigo em Espanhol | MEDLINE | ID: mdl-10410592

RESUMO

The investigations of mitochondrial DNA abnormalities and its relationship with derangements of oxidative phosphorylation and electron transport system, has yielded description a myriad of syndromes called mitochondrial diseases or cytopathies. The objective of this paper is to review the clinical relevant features of this heterogeneous group of diseases, to understand the board spectrum of signs and symptoms and suggest an algorithm for the diagnosis.


Assuntos
DNA Mitocondrial/genética , Genoma , Miopatias Mitocondriais/genética , Fosforilação Oxidativa , Cardiomiopatias/genética , Diagnóstico Diferencial , Herança Extracromossômica , Feminino , Humanos , Ácido Láctico/sangue , Masculino , Miopatias Mitocondriais/diagnóstico , Atrofias Ópticas Hereditárias/genética , Fenótipo , Ácido Pirúvico/sangue
6.
Arch Inst Cardiol Mex ; 69(6): 559-65, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10742853

RESUMO

Kearns-Sayre syndrome is a mitochondrial cytopathy characterized by chronic progressive external ophthalmoplegia, retinitis pigmentosa and heart block, the last of which determines the survival of these patients. The case of a 23 year old man with Kearns-Sayre syndrome, conduction disturbances and mitral valve prolapse is presented. The characteristics of this syndrome are described and the criteria for prophylactic installation of a pacemaker discussed.


Assuntos
Síndrome de Kearns-Sayre/terapia , Marca-Passo Artificial , Adulto , Bloqueio de Ramo/prevenção & controle , Humanos , Masculino
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