Vascular perfusion abnormalities in infants with spinal muscular atrophy
- PMID: 19619755
- PMCID: PMC3250227
- DOI: 10.1016/j.jpeds.2009.01.071
Vascular perfusion abnormalities in infants with spinal muscular atrophy
Abstract
Spinal muscular atrophy (SMA) is an important cause of death in children and SMA type I, also known as Werdnig-Hoffman disease, is the most severe form of this disease. We report 2 cases of infants with SMA I in whom a distal necrosis developed, a feature not previously reported. Poor perfusion, autonomic dysfunction, and position-dependent factors may all play a role in the development of this complication.
Conflict of interest statement
The authors declare no conflicts of interest.
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References
-
- Bach JR. Medical considerations of long-term survival of Werdnig-Hoffmann disease. Am J Phys Med Rehabil. 2007;86:349–355. - PubMed
-
- Oskoui M, Levy G, Garland CJ, Gray JM, O’Hagen J, De Vivo DC. The changing natural history of spinal muscular atrophy type 1. Neurology. 2007;69:1931–1936. - PubMed
-
- Lambrechts D, Carmeliet P. VEGF at the neurovascular interface: Therapeutic implications for motor neuron disease. Biochimica et Biophysica Acta. 2006;1762:1109–1121. - PubMed
-
- Dettmers C, Fatepour D, Faust H, Jerusalem F. Sympathetic skin response abnormalities in amyotrophic lateral sclerosis. Muscle Nerve. 1993;16:930–934. - PubMed
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