Pediatric Neurology Briefs (Aug 1988)

Multiple Sulfatase Deficiency

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-2-8-2
Journal volume & issue
Vol. 2, no. 8
pp. 58 – 58

Abstract

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A 9-year-old girl with a phenotype similar to a mucopolysaccharidosis (MPS) and a clinical history characteristic of late infantile metachromatic leukodystrophy (MLD) is reported from the Department of Neurology, National Defense Medical Center, Taipei, Taiwan, Republic of China; the Developmental and Metabolic Neurology Branch, NIH, Bethesda, Maryland; and Department of Pediatrics (Dr. Horwitz), University of Chicago, Chicago, Illinois.

Keywords