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1.
Australas J Dermatol ; 63(1): e75-e77, 2022 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-34817065

RESUMO

Calciphylaxis is a potencially disorder in patients with hyperphosphatemic familial tumoral calcinosis (HFTC). Patients commonly present livedo racemosa and retiform purpura, which may progress to necrosis and very painful ulcers. Treatment with sodium thiosulfate provides good results; however, intralesional and intravenous treatment can be limited by its adverse effects. Topical sodium thiosulfate has been successfully reported for cutaneous calcification associated with connective tissue diseases and calciphylaxis in patients with chronic kidney disease. We provide a case report of a patient with HFTC and calciphylaxis who was treated with topical sodium thiosulfate with a rapid and complete response with no side effects.


Assuntos
Antioxidantes/uso terapêutico , Calcinose/tratamento farmacológico , Calciofilaxia/tratamento farmacológico , Hiperostose Cortical Congênita/tratamento farmacológico , Hiperfosfatemia/tratamento farmacológico , Tiossulfatos/uso terapêutico , Idoso , Humanos , Masculino
2.
Hum Immunol ; 78(5-6): 435-440, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28259733

RESUMO

The IκBζ protein (NFKBIZ gene) is a nuclear inhibitor of NF-κB and plays an important role in the pathogenesis of Psoriasis (Psor). We sought to determine whether common NFKBIZ variants were associated with the risk of developing Psor. A total of 392 patients and 336 controls were genotyped for a common intron 10 indel that could affect pre-mRNA splicing. We found a significantly higher frequency of the insertion among the cw6-positive patients (p=0.01). Cw6-positive+intron 10 ins/ins were significantly more frequent in the patients (OR=3.61). The analysis of the cDNA from leukocytes showed a NFKBIZ transcript lacking exon 10, present in all the tested samples. This new alternative transcript lacks a domain predicted to interact with the NFKB1/p50 protein. Functional studies to define the effect of this alternative transcript on the regulation of the NF-κB pathway are necessary.


Assuntos
Genótipo , Proteínas I-kappa B/genética , Leucócitos/fisiologia , Mutação/genética , Proteínas Nucleares/genética , Psoríase/genética , Proteínas Adaptadoras de Transdução de Sinal , Adulto , Células Cultivadas , Feminino , Estudos de Associação Genética , Predisposição Genética para Doença , Humanos , Masculino , Pessoa de Meia-Idade , NF-kappa B/metabolismo , Polimorfismo Genético , Ligação Proteica/genética , Splicing de RNA , Risco , Transdução de Sinais , Espanha
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