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Adverse environmental conditions influence age-related innate immune responsiveness
Authors:Linda May  Anita HJ van den Biggelaar  David van Bodegom  Hans J Meij  Anton JM de Craen  Joseph Amankwa  Marijke Frölich  Maris Kuningas  Rudi GJ Westendorp
Affiliation:1. Laboratório de Pesquisa em Produtos Naturais, Departamento de Ciências físicas e Biológicas, Centro de Ciências Biológicas e da Saúde, Universidade Regional do Cariri, Crato (CE), Brazil
2. Laboratório de Genética de Microrganismos, Departamento de Biologia Molecular, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba, Jo?o Pessoa (PB), Brazil
3. Laboratório de Bioquímica, Genética e Radiobiologia, Departamento de Biologia Molecular, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba, Jo?o Pessoa (PB), Brazil
Abstract:Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature aging disorder that belongs to a group of conditions called laminopathies which affect nuclear lamins. Mutations in two genes, LMNA and ZMPSTE24, have been found in patients with HGPS. The p.G608G LMNA mutation is the most commonly reported mutation. The aim of this work was to compile a comprehensive literature review of the clinical features and genetic mutations and mechanisms of this syndrome as a contribution to health care workers. This review shows the necessity of a more detailed clinical identification of Hutchinson-Gilford progeria syndrome and the need for more studies on the pharmacologic and pharmacogenomic approach to this syndrome.
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