Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome

• Autor(es): Navarro, D ; Azevedo, A ; Sequeira, S ; Ferreira, AC ; Carvalho, F ; Fidalgo, T ; Vilarinho, L ; Santos, MC ; Calado, J ; Nolasco, F
• Data: 2018
• Identificador Persistente: http://hdl.handle.net/10400.4/2181
• Origem: Repositório do Centro Hospitalar e Universitário de Coimbra
• Assunto(s): Síndrome Hemolítico-Urémico Atípico; Erros Inatos do Metabolismo dos Aminoácidos; Ácido Metilmalónico
• Tipo de Documento: Artigo científico
• Idioma: Inglês
• Contribuidor(es): RIHUC

Descrição

Thrombotic microangiopathy (TMA) syndromes can be secondary to a multitude of different diseases. Most can be identified with a systematic approach and, when excluded, TMA is generally attributed to a dysregulation in the activity of the complement alternative pathways-atypical hemolytic uremic syndrome (aHUS). We present a challenging case of a 19-year-old woman who presented with thrombotic microangiopathy, which was found to be caused by methylmalonic acidemia and homocystinuria, a rare vitamin B12 metabolism deficiency. To our knowledge, this is the first time that an adult-onset methylmalonic acidemia and homocystinuria presents as TMA preceding CNS involvement.