Rhizomelic chondrodysplasia punctata is a rare genetic disorder of peroxisomal metabolism that is characterized clinically by shortening of the proximal limbs, cataracts, a characteristic facial appearance, failure to thrive, and psychomotor retardation. This report describes a newborn with a severe phenotype whose neuroimaging showed pachygyria-polymicrogyria, severe spinal stenosis causing compression of the cervical cord and brainstem, and tethering of the spinal cord. Imaging of the brain and spinal cord in patients with this disorder may aid prognosis and guide management decisions. (C) 2007 by Elsevier Inc. All rights reserved.
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Univ Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Neurol, NL-1105 AZ Amsterdam, NetherlandsUniv Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Neurol, NL-1105 AZ Amsterdam, Netherlands
Bams-Mengerink, Annemieke M.
Koelman, Johannes H. T. M.
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Acad Med Ctr Amsterdam, Dept Neurol, Amsterdam, NetherlandsUniv Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Neurol, NL-1105 AZ Amsterdam, Netherlands
Koelman, Johannes H. T. M.
Waterham, Hans
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Acad Med Ctr Amsterdam, Lab Genet Metab Dis, Amsterdam, NetherlandsUniv Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Neurol, NL-1105 AZ Amsterdam, Netherlands
Waterham, Hans
Barth, Peter G.
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Univ Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Neurol, NL-1105 AZ Amsterdam, NetherlandsUniv Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Neurol, NL-1105 AZ Amsterdam, Netherlands