Literature DB >> 6738841

Computed tomography in late-onset metachromatic leucodystrophy.

H I Schipper, D Seidel.   

Abstract

In late-onset metachromatic leucodystrophy (MLD), early clinical diagnosis is difficult since initial symptoms frequently consist of misleading nonspecific psychopathological alterations. On cranial computed tomography (CT), however, symmetrical attenuation decrease of the white matter and mild cerebral atrophy can already be found in an early stage of the disease, and may even precede clinical symptoms. On the basis of observations in four patients with late-onset MLD who were followed between 1 and 5 years, characteristic CT appearances in different stages of the disease are outlined and compared with the literature.

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Year:  1984        PMID: 6738841     DOI: 10.1007/BF00328202

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  12 in total

1.  [Procedure for the diagnosis of sphingolipidoses or allied diseases in adult patients with neurological or psychiatric symptoms (author's transl)].

Authors:  H Pilz; R Heipertz; D Seidel
Journal:  Nervenarzt       Date:  1979-12       Impact factor: 1.214

2.  [Computerized tomography in neurodegenerative diseases in childhood (author's transl)].

Authors:  F Kotlarek; H Zeumer
Journal:  Monatsschr Kinderheilkd       Date:  1979-09

3.  Late-onset metachromatic leukodystrophy: diagnostic problems elucidated by a case report.

Authors:  D Seidel; H H Goebel; W Scholz
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

4.  Demyelinating and neuro-degenerative disease in childhood. CT appearances and their differential diagnosis.

Authors:  D P Kingsley; B E Kendall
Journal:  J Neuroradiol       Date:  1981       Impact factor: 3.447

5.  Computed tomography in neurodegenerative disorders in childhood.

Authors:  E Boltshauser; H Spiess; W Isler
Journal:  Neuroradiology       Date:  1978       Impact factor: 2.804

6.  White-gray matter differentiation in computed tomography.

Authors:  T Arimitsu; G Di Chiro; R A Brooks; P B Smith
Journal:  J Comput Assist Tomogr       Date:  1977-10       Impact factor: 1.826

7.  Computed tomography in late-infantile metachromatic leukodystrophy.

Authors:  F S Buonanno; M R Ball; D W Laster; D M Moody; W T McLean
Journal:  Ann Neurol       Date:  1978-07       Impact factor: 10.422

8.  Computed tomography in white-matter disease.

Authors:  E R Heinz; B P Drayer; C A Haenggeli; M J Painter; P Crumrine
Journal:  Radiology       Date:  1979-02       Impact factor: 11.105

9.  Computerized tomography in demyelinating disease of the young.

Authors:  W C Robertson; M R Gomez; D F Reese; H Okazaki
Journal:  Neurology       Date:  1977-09       Impact factor: 9.910

10.  Computerised tomography in the leucodystrophies.

Authors:  P G Procopis
Journal:  Clin Exp Neurol       Date:  1979
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  10 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

Review 2.  Psychiatric symptoms of inherited metabolic disease.

Authors:  Y Estrov; F Scaglia; O A Bodamer
Journal:  J Inherit Metab Dis       Date:  2000-02       Impact factor: 4.982

3.  Adult metachromatic leucodystrophy: an underdiagnosed disease?

Authors:  M Cerizza; R Nemni; F Tamma
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-12       Impact factor: 10.154

4.  Metachromatic leukodystrophy: conduct disorder progressing to dementia.

Authors:  N R Fisher; S J Cope; W A Lishman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-04       Impact factor: 10.154

5.  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

6.  Adult-onset metachromatic leucodystrophy presenting without psychiatric symptoms.

Authors:  E Klemm; E Conzelmann
Journal:  J Neurol       Date:  1989-10       Impact factor: 4.849

7.  Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications.

Authors:  C Hohenschutz; P Eich; W Friedl; A Waheed; E Conzelmann; P Propping
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

8.  Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults.

Authors:  M S van der Knaap; J Valk; N de Neeling; J J Nauta
Journal:  Neuroradiology       Date:  1991       Impact factor: 2.804

9.  Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease.

Authors:  J M Penzien; J Kappler; N Herschkowitz; B Schuknecht; P Leinekugel; P Propping; T Tønnesen; H Lou; H Moser; S Zierz
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

10.  The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patients.

Authors:  P Propping; W Friedl; M Huschka; K H Schlör; F Reimer; M Lee-Vaupel; E Conzelmann; K Sandhoff
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

  10 in total

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