Rare inherited kidney diseases: an evolving field in Nephrology

• Autor(a) principal: Cunha,Mariana Faucz Munhoz da
• Data de Publicação: 2020
• Outros Autores: Sevignani,Gabriela, Pavanelli,Giovana Memari, Carvalho,Mauricio de, Barreto,Fellype Carvalho
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Jornal Brasileiro de Nefrologia
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002020000200219
• topic: Genetic Diseases, Inborn; Kidney Diseases; Glomerulosclerosis, Focal Segmental; Fabry Disease; Tuberous Sclerosis

Abstract There are more than 150 different rare genetic kidney diseases. They can be classified according to diagnostic findings as (i) disorders of growth and structure, (ii) glomerular diseases, (iii) tubular, and (iv) metabolic diseases. In recent years, there has been a shift of paradigm in this field. Molecular testing has become more accessible, our understanding of the underlying pathophysiologic mechanisms of these diseases has evolved, and new therapeutic strategies have become more available. Therefore, the role of nephrologists has progressively shifted from a mere spectator to an active player, part of a multidisciplinary team in the diagnosis and treatment of these disorders. This article provides an overview of the recent advances in rare hereditary kidney disorders by discussing the genetic aspects, clinical manifestations, diagnostic, and therapeutic approaches of some of these disorders, named familial focal and segmental glomerulosclerosis, tuberous sclerosis complex, Fabry nephropathy, and MYH-9 related disorder.