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1.
Eur J Med Genet ; 59(4): 219-22, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26853951

RESUMO

Human immunoglobulin molecules are generated by a pair of identical heavy chains, which identify the immunoglobulin class, and a pair of identical light chains, Kappa or Lambda alternatively, which characterize the immunoglobulin type. In normal conditions, Kappa light chains represent approximately 2/3 of the light chains of total immunoglobulins, both circulating and lymphocyte surface bound. Very few cases of immunoglobulin Kappa or Lambda light chain defects have been reported. Furthermore, the genetic basis of this defect has been extensively explored only in a single case. We report a case of a patient suffering of serious recurrent bacterial infections, which was caused by a very rare form of immunoglobulin disorder, consisting of a pure defect of Kappa light chain. We evaluated major serum immunoglobulin concentrations, as well as total and free Kappa and Lambda light chain concentrations. Lymphocyte phenotyping was also performed and finally we tested the Kappa chain VJ rearrangement as well as the constant Kappa region sequence. Studies performed on VJ rearrangement showed a polyclonal genetic arrangement, whereas the gene sequencing for the constant region of Kappa chain showed a homozygous T to G substitution at the position 1288 (rs200765148). This mutation causes a substitution from Cys to Gly in the protein sequence and, therefore, determines the abnormal folding of the constant region of Kappa chain. We suggest that this defect could lead to an effective reduction of the variability of total antibody repertoire and a consequent defect of an apparently normal immunoglobulin response to common antigens.


Assuntos
Imunidade Humoral/genética , Cadeias kappa de Imunoglobulina/genética , Cadeias lambda de Imunoglobulina/genética , Síndromes de Imunodeficiência/genética , Sequência de Aminoácidos/genética , Feminino , Humanos , Síndromes de Imunodeficiência/patologia , Linfócitos/patologia , Pessoa de Meia-Idade
2.
J Forensic Leg Med ; 34: 81-7, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26165664

RESUMO

Sudden deaths attributed to sniffing trichloroethylene are caused by the abuse of this solvent which produces pleasant inebriating effects with rapid dissipation. In the event of repeated cycles of inhalation, a dangerous and uncontrolled systemic accumulation of trichloroethylene may occur, followed by central nervous system depression, coma and lethal cardiorespiratory arrest. Sometimes death occurs outside the hospital environment, without medical intervention or witnesses and without specific necroscopic signs. Medico legal investigations into sudden sniffing deaths associated with trichloroethylene demand careful analysis of the death scene and related circumstances, a detailed understanding of the deceased's medical history and background of substance abuse and an accurate evaluation of all autopsy and laboratory data, with close cooperation between the judiciary, coroners and toxicologists.


Assuntos
Morte Súbita/etiologia , Abuso de Inalantes/diagnóstico , Solventes/intoxicação , Tricloroetileno/intoxicação , Arritmias Cardíacas/induzido quimicamente , Catecolaminas/biossíntese , Vasoespasmo Coronário/induzido quimicamente , Toxicologia Forense , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Abuso de Inalantes/complicações , Solventes/análise , Solventes/farmacocinética , Manejo de Espécimes , Detecção do Abuso de Substâncias , Tricloroetileno/análise , Tricloroetileno/farmacocinética
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