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Long-Term Survival in a Child With Arthrogryposis Multiplex Congenita and Spinal Muscular AtrophyDepartment of Pediatrics, Azienda Policlinico Division of Pediatric Neurology, Azienda Policlinico University of Catania Sicily, Italy
Department of Pediatrics, Azienda Policlinico Division of Pediatric Neurology, Azienda Policlinico University of Catania Sicily, Italy
Department of Pediatrics, Azienda Policlinico Division of Pediatric Neurology, Azienda Policlinico University of Catania Sicily, Italy
Department of Pediatrics, Azienda Policlinico Division of Pediatric Neurology, Azienda Policlinico University of Catania Sicily, Italy
Institute of Bioimaging and Physiopathology of the Central Nervous System CNR National Research Council of Italy Catania, Italy
Department of Neurology and Pediatrics St. Louis Children's Hospital Washington School of Medicine , St. Louis, Missouri, connolly{at}kids.wustl.edu 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. (J Child Neurol 2001;16:934-936).
Journal of Child Neurology, Vol. 16, No. 12,
934-936 (2001) |
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