Literature DB >> 2809646

Adult-onset metachromatic leucodystrophy presenting without psychiatric symptoms.

E Klemm1, E Conzelmann.   

Abstract

A 24-year-old man presented with a spastic and ataxic condition resembling chronic-progressive multiple sclerosis. Radiological examination revealed symmetrical diffuse paraventricular demyelination. Electrophysiological findings suggested additional involvement of the brain stem and the peripheral nervous system. The diagnosis of adult-onset metachromatic leucodystrophy was confirmed by biochemical and ultrastructural examination. In contrast to almost all adult cases reported so far, psychiatric symptoms were not present.

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Year:  1989        PMID: 2809646     DOI: 10.1007/bf00314905

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  6 in total

1.  Studies on adult metachromatic leukodystrophy. 1. Clinical, morphological and histochemical observations in two cases.

Authors:  D Müller; H Pilz; V ter Meulen
Journal:  J Neurol Sci       Date:  1969 Nov-Dec       Impact factor: 3.181

2.  Assay for cerebroside sulfate (sulfatide) sulfatase in cultured skin fibroblasts with the natural activator protein.

Authors:  M Lee-Vaupel; E Conzelmann
Journal:  Clin Chim Acta       Date:  1987-09-15       Impact factor: 3.786

3.  Computed tomography in late-onset metachromatic leucodystrophy.

Authors:  H I Schipper; D Seidel
Journal:  Neuroradiology       Date:  1984       Impact factor: 2.804

4.  Metachromatic leukodystrophy (MLD). 8. MLD in adults; diagnosis and pathogenesis.

Authors:  J Austin; D Armstrong; S Fouch; C Mitchell; D Stumpf; L Shearer; O Briner
Journal:  Arch Neurol       Date:  1968-03

5.  Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis.

Authors:  R Eldridge; C P Anayiotos; S Schlesinger; D Cowen; C Bever; N Patronas; H McFarland
Journal:  N Engl J Med       Date:  1984-10-11       Impact factor: 91.245

  6 in total
  3 in total

Review 1.  Metachromatic leukodystrophy: a case of triplets with the late infantile variant and a systematic review of the literature.

Authors:  Asif Mahmood; Jay Berry; David A Wenger; Maria Escolar; Magdi Sobeih; Gerald Raymond; Florian S Eichler
Journal:  J Child Neurol       Date:  2009-12-28       Impact factor: 1.987

2.  Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.

Authors:  J Kappler; P Leinekugel; E Conzelmann; W J Kleijer; A Kohlschütter; T Tønnesen; M Rochel; F Freycon; P Propping
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

3.  Case Report: Novel Arylsulfatase A (ARSA) Gene Mutations in a Patient With Adult-Onset Metachromatic Leukodystrophy Misdiagnosed as Multiple Sclerosis.

Authors:  Lulu Xu; Meixiang Zhong; Yajuan Wang; Zhihong Wang; Jie Song; Jing Zhao; Hongyun Yu; Zhencui Yang; Wenjing Yan; Xueping Zheng
Journal:  Front Neurol       Date:  2021-01-11       Impact factor: 4.003

  3 in total

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