Literature DB >> 15644995

Adult metachromatic leukodystrophy: disorganized schizophrenia-like symptoms and postpartum depression in 2 sisters.

Hojka Gregoric Kumperscak1, Eduard Paschke, Peter Gradisnik, Jernej Vidmar, Stanislava Umek Bradac.   

Abstract

We describe the cases of 2 sisters with adult metachromatic leukodystrophy (MLD). Whereas one sister presented with disorganized schizophrenia-like symptoms as the initial manifestation of MLD, the other remained symptom free except for a 4-week period of postpartum depression. In both patients, there was some residual activity of leukocyte arylsulfatase A (1.7% and 5.5% of normal), and a marked increase in urinary sulfatides was present, as measured by tandem mass spectrometry. An arylsulfatase A pseudodeficiency was therefore excluded. The most common mutations of the adult phenotype, Ile-179-Ser and Pro-426-Leu, were not found. In the literature, only 1 case of adult MLD manifesting as disorganized schizophrenia-like symptoms has been described, whereas postpartum depression has been so far unknown as a presenting symptom of MLD.

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Year:  2005        PMID: 15644995      PMCID: PMC543838     

Source DB:  PubMed          Journal:  J Psychiatry Neurosci        ISSN: 1180-4882            Impact factor:   6.186


  12 in total

1.  Characterization of urinary sulfatides in metachromatic leukodystrophy using electrospray ionization-tandem mass spectrometry.

Authors:  P D Whitfield; P C Sharp; D W Johnson; P Nelson; P J Meikle
Journal:  Mol Genet Metab       Date:  2001-05       Impact factor: 4.797

2.  A novel arylsulfatase A protein variant and genotype in two patients with major depression.

Authors:  M H Ricketts; J D Amsterdam; D S Park; R S Yang; R D Poretz; X Zhang; M Fanale; A Baddoo; P Manowitz
Journal:  J Affect Disord       Date:  1996-10-14       Impact factor: 4.839

3.  Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer.

Authors:  W Rommerskirch; A L Fluharty; C Peters; K von Figura; V Gieselmann
Journal:  Biochem J       Date:  1991-12-01       Impact factor: 3.857

4.  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

5.  [Homicide and hebephrenia-like syndrome in metachromatic leukodystrophy].

Authors:  M Rentrop; K Hakk; F J Freisleder; W Kissling; G Kockott
Journal:  Nervenarzt       Date:  1999-03       Impact factor: 1.214

Review 6.  Update on genetic disorders affecting white matter.

Authors:  E M Kaye
Journal:  Pediatr Neurol       Date:  2001-01       Impact factor: 3.372

7.  Late juvenile metachromatic leukodystrophy (MLD) in three patients with a similar clinical course and identical mutation on one allele.

Authors:  A Tylki-Szymanska; J Berger; B Löschl; A Lugowska; B Molzer
Journal:  Clin Genet       Date:  1996-11       Impact factor: 4.438

8.  Adult metachromatic leukodystrophy: three cases with normal nerve conduction velocities in a family.

Authors:  N Cengiz; T Ozbenli; M Onar; L Yildiz; B Ertaş
Journal:  Acta Neurol Scand       Date:  2002-06       Impact factor: 3.209

9.  Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiency.

Authors:  A T Hageman; F J Gabreëls; J G de Jong; A A Gabreëls-Festen; C J van den Berg; B A van Oost; R A Wevers
Journal:  Arch Neurol       Date:  1995-04

10.  Late juvenile metachromatic leukodystrophy treated with bone marrow transplantation; a 4-year follow-up study.

Authors:  C Navarro; J M Fernández; C Domínguez; C Fachal; M Alvarez
Journal:  Neurology       Date:  1996-01       Impact factor: 9.910

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  6 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.  Lysosomal storage diseases--the horizon expands.

Authors:  Rose-Mary Naaman Boustany
Journal:  Nat Rev Neurol       Date:  2013-08-13       Impact factor: 42.937

3.  Diffusion and ADC-map images detect ongoing demyelination on subcortical white matter in an adult metachromatic leukodystrophy patient with autoimmune Hashimoto thyroiditis.

Authors:  Akiko Miura; Yuri Kumabe; En Kimura; Satoshi Yamashita; Akihiko Ueda; Teruyuki Hirano; Makoto Uchino
Journal:  BMJ Case Rep       Date:  2010-12-01

Review 4.  Psychiatric signs and symptoms in treatable inborn errors of metabolism.

Authors:  S Nia
Journal:  J Neurol       Date:  2014-09       Impact factor: 4.849

5.  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

Review 6.  Metachromatic Leukodystrophy: Diagnosis, Modeling, and Treatment Approaches.

Authors:  Alisa A Shaimardanova; Daria S Chulpanova; Valeriya V Solovyeva; Aysilu I Mullagulova; Kristina V Kitaeva; Cinzia Allegrucci; Albert A Rizvanov
Journal:  Front Med (Lausanne)       Date:  2020-10-20
  6 in total

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