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Research ArticlePEDIATRIC

MR Brain Imaging of Fucosidosis Type I

Paolo Galluzzi, Alessandra Rufa, Paolo Balestri, Alfonso Cerase and Antonio Federico
American Journal of Neuroradiology April 2001, 22 (4) 777-780;
Paolo Galluzzi
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Alessandra Rufa
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Paolo Balestri
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Alfonso Cerase
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Antonio Federico
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Abstract

Summary: Fucosidosis is a rare autosomal recessive lysosomal storage disease with the main clinical findings of progressive neuromotor deterioration, seizures, coarse facial features, dysostosis multiplex, angiokeratoma corporis diffusum, visceromegaly, recurrent respiratory infections, and growth retardation. Fucosidosis type I rapidly evolves toward a progressive neurologic deterioration and death. We report MR imaging findings of the brain of three patients with fucosidosis type I, including previously unreported findings, to expand the knowledge of the neuroradiologic spectrum of the disease.

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American Journal of Neuroradiology
Vol. 22, Issue 4
1 Apr 2001
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Cite this article
Paolo Galluzzi, Alessandra Rufa, Paolo Balestri, Alfonso Cerase, Antonio Federico
MR Brain Imaging of Fucosidosis Type I
American Journal of Neuroradiology Apr 2001, 22 (4) 777-780;

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MR Brain Imaging of Fucosidosis Type I
Paolo Galluzzi, Alessandra Rufa, Paolo Balestri, Alfonso Cerase, Antonio Federico
American Journal of Neuroradiology Apr 2001, 22 (4) 777-780;
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Cited By...

  • A novel homozygous frameshift mutation in the FUCA1 gene causes both severe and mild fucosidosis
  • A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease
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