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Severe brain involvement in 5q spinal muscular atrophy type 0.
Mendonça, Rodrigo H; Rocha, Antônio J; Lozano-Arango, Andres; Diaz, Astry B; Castiglioni, Claudia; Silva, André M S; Reed, Umbertina C; Kulikowski, Leslie; Paramonov, Ida; Cuscó, Ivon; Tizzano, Eduardo F; Zanoteli, Edmar.
Afiliación
  • Mendonça RH; Department of Neurology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
  • Rocha AJ; Neuroradiology Section, High Diagnostic Excellence (DASA Group), São Paulo, Brazil.
  • Lozano-Arango A; Hernan Henriquez Aravena Regional Hospital, Temuco, Chile.
  • Diaz AB; Hernan Henriquez Aravena Regional Hospital, Temuco, Chile.
  • Castiglioni C; Department of Pediatric Neurology, Las Condes Clinic, Santiago, Chile.
  • Silva AMS; Department of Neurology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
  • Reed UC; Department of Neurology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
  • Kulikowski L; Department of Pathology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
  • Paramonov I; Department of Clinical and Molecular Genetics, Valle Hebron University Hospital, Medicine Genetics Group, Valle Hebron Research Institute, Barcelona, Spain.
  • Cuscó I; Department of Clinical and Molecular Genetics, Valle Hebron University Hospital, Medicine Genetics Group, Valle Hebron Research Institute, Barcelona, Spain.
  • Tizzano EF; Department of Clinical and Molecular Genetics, Valle Hebron University Hospital, Medicine Genetics Group, Valle Hebron Research Institute, Barcelona, Spain.
  • Zanoteli E; Department of Neurology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.
Ann Neurol ; 86(3): 458-462, 2019 09.
Article en En | MEDLINE | ID: mdl-31301241
ABSTRACT
Spinal muscular atrophy (SMA) type 0 is the most severe form of SMA, associated with the SMN1 gene and manifesting at birth. Most patients die in the first weeks of life. In this work, we present 3 patients with SMA type 0 who survived >1 year and presented diffuse and progressive brain abnormalities on magnetic resonance imaging, which are not usually seen in patients with SMA. Thus, severe brain involvement may likely be the full end manifestation of an already extreme SMA phenotype caused by substantial reduction of the SMN protein in the brain. ANN NEUROL 2019;86458-462.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Atrofia Muscular Espinal Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Ann Neurol Año: 2019 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Atrofia Muscular Espinal Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Ann Neurol Año: 2019 Tipo del documento: Article País de afiliación: Brasil