| Literature DB >> 11061266 |
K J Felice1, M Gomez Lira, M Natowicz, M L Grunnet, G J Tsongalis, A A Sima, R F Kaplan.
Abstract
A 22-year-old man presented with recurrent ulnar mononeuropathies and diffusely slow nerve conduction velocities. Arylsulfatase A (ASA) activity from leukocytes and fibroblasts was reduced, and urinary sulfatides were increased. Sural nerve biopsy revealed a reduction in myelinated fibers and Schwann cell inclusions. Results of studies of CNS integrity, including cranial MRI, evoked potentials, and neuropsychologic tests, were normal. Molecular genetic analyses revealed a novel homozygous missense mutation (Thr286Pro) in the ASA gene.Entities:
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Year: 2000 PMID: 11061266 DOI: 10.1212/wnl.55.7.1036
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910