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Long-term survival in a child with arthrogryposis multiplex congenita and spinal muscular atrophy.
Falsaperla, R; Romeo, G; Di Giorgio, A; Pavone, P; Parano, E; Connolly, A M.
Afiliação
  • Falsaperla R; Department of Pediatrics, Azienda Policlinico, University of Catania, Sicily, Italy.
J Child Neurol ; 16(12): 934-6, 2001 Dec.
Article em En | MEDLINE | ID: mdl-11785510
ABSTRACT
Spinal muscular atrophy type 0 is a severe form of spinal muscular atrophy that is usually fatal in the first months of life. These children present with arthrogryposis multiplex congenita and respiratory compromise. We describe a child with spinal muscular atrophy and arthrogryposis multiplex congenita who has had a much better course and is alive without ventilator support at age 6 years. This case illustrates that the prognosis for spinal muscular atrophy and arthrogryposis multiplex congenita cannot always be predicted with certainty.
Assuntos
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Base de dados: MEDLINE Assunto principal: Artrogripose / Atrofias Musculares Espinais da Infância Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Revista: J Child Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Itália
Buscar no Google
Base de dados: MEDLINE Assunto principal: Artrogripose / Atrofias Musculares Espinais da Infância Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Revista: J Child Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Itália