Literature DB >> 2877931

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

P Propping, W Friedl, M Huschka, K H Schlör, F Reimer, M Lee-Vaupel, E Conzelmann, K Sandhoff.   

Abstract

A total of 1728 patients consecutively admitted to a neuropsychiatric hospital and 379 chronically ill inpatients were examined for activity of arylsulphatase A (ASA) in leucocytes. A further 519 healthy individuals served as controls. We did not find evidence for the involvement of low ASA activity in chronic patients. The consecutive admissions showed a slight preponderance in the lower ASA activity classes. This activity range covers persons heterozygous for ASA deficiency alleles. The data are compatible with the hypothesis that carriers of low ASA activity alleles are at a slightly higher risk for neuropsychiatric disorders.

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Year:  1986        PMID： 2877931     DOI： 10.1007/bf00282542

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  45 in total

1.  A CONTROLLED STUDY OF ENZYMIC ACTIVITIES IN THREE HUMAN DISORDERS OF GLYCOLIPID METABOLISM.

Authors:  J H AUSTIN; A S BALASUBRAMANIAN; T N PATTABIRAMAN; S SARASWATHI; D K BASU; B K BACHHAWAT
Journal:  J Neurochem       Date:  1963-12       Impact factor: 5.372

2.  [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

3.  A variant form of metachromatic leukodystrophy without arylsulfatase deficiency.

Authors:  A F Hahn; B A Gordon; G G Hinton; J J Gilbert
Journal:  Ann Neurol       Date:  1982-07       Impact factor: 10.422

4.  Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.

Authors:  H Kihara; A L Fluharty; J S O'Brien; C H Fish
Journal:  Clin Genet       Date:  1982-04       Impact factor: 4.438

Review 5.  Clinical consequences of heterozygosity for autosomal-recessive diseases.

Authors:  F Vogel
Journal:  Clin Genet       Date:  1984-05       Impact factor: 4.438

6.  Diagnosis of gaucher's disease and niemann-pick disease with small samples of venous blood.

Authors:  J P Kampine; R O Brady; J N Kanfer; M Feld; D Shapiro
Journal:  Science       Date:  1967-01-06       Impact factor: 47.728

7.  Non-progressive psychomotor retardation in a child with severe deficiency of arylsulphatase A activity.

Authors:  C Danesino; A D'Azzo; M Aricò; A F Podestà; G Beluffi; E Bianchi
Journal:  Clin Genet       Date:  1984-11       Impact factor: 4.438

8.  Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis.

Authors:  T Tønnesen; C Vrang; U N Wiesmann; H Christomanou; H O Lou
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  A variant form of metachromatic leucodystrophy in a patient suffering from another congenital degenerative neurological disease.

Authors:  A M Nordenbo; T Tønnesen
Journal:  Acta Neurol Scand       Date:  1985-01       Impact factor: 3.209
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  6 in total

1.  Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy.

Authors:  H Kohn; P Manowitz; M Miller; A Kling
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

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.  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

4.  Extremely low arylsulfatase A enzyme activity does not necessarily cause symptoms: A long-term follow-up and review of the literature.

Authors:  Lucia Laugwitz; Vidiyaah Santhanakumaran; Mareike Spieker; Judith Boehringer; Benjamin Bender; Volkmar Gieselmann; Stefanie Beck-Woedl; Gernot Bruchelt; Klaus Harzer; Ingeborg Kraegeloh-Mann; Samuel Groeschel
Journal:  JIMD Rep       Date:  2022-05-04

5.  Myoclonic epilepsy of Lafora and arylsulphatase A deficiency in the same patient.

Authors:  B Bertagnolio; F Girotti; D Pelucchetti; M Pandolfo
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

6.  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
  6 in total

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