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Review
. 2023 Oct;32(10):2043-2047.
doi: 10.1007/s00787-022-02031-5. Epub 2022 Jul 7.

Psychiatric symptoms in Salla disease

Affiliations
Review

Psychiatric symptoms in Salla disease

Ida Aulanko et al. Eur Child Adolesc Psychiatry. 2023 Oct.

Abstract

Salla disease (SD) is a rare lysosomal storage disorder characterised by intellectual disability ataxia, athetosis, nystagmus, and central nervous system demyelination. Although the neurological spectrum of SD's clinical phenotype is well defined, psychotic symptoms in SD remain unreported. We reviewed the presence of psychiatric symptoms in patients diagnosed with SD. Medical records of all SD patients at Oulu University Hospital during the years 1982-2015 were systematically reviewed to evaluate the presence of psychiatric symptoms. Psychiatric symptoms were frequently associated with SD (10/24, 42%), and two patients were described as developing psychosis as adolescents. We reported their clinical characteristics in detail and assessed the prevalence of psychiatric symptoms in a cohort of 24 patients. Other psychiatric factors associated with SD were sleeping disorders (8/24, 32%), aggressive behaviour disorders or restlessness (6/24, 25%), and off-label antipsychotic medication (4/24, 17%). This report expands the knowledge of the phenotypic spectrum of SD and demonstrates the importance of recognising the possibility of psychiatric symptoms, including psychosis, in persons with SD.

Keywords: Behaviour disorder; Clinical report; Organic psychosis; Register-based study; Salla disease; Sialuria; Sleeping disorder.

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Conflict of interest statement

The authors disclose no conflicts of interest.

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References

    1. Aula P, Autio S, Raivio KO, Rapola J, Thodén C-J, Koskela S-L, et al. “Salla Disease”: a new lysosomal storage disorder. Arch Neurol. 1979;36:88–94. doi: 10.1001/archneur.1979.00500380058006. - DOI - PubMed
    1. Renlund M, Aula P, Raivio KO, Autio S, Sainio K, Rapola J, et al. Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolism. Neurology. 1983;33:57. doi: 10.1212/WNL.33.1.57. - DOI - PubMed
    1. Verheijen FW, Verbeek E, Aula N, Beerens CEMT, Havelaar AC, Joosse M, et al. A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. Nat Genet. 1999;23:462–465. doi: 10.1038/70585. - DOI - PubMed
    1. Barmherzig R, Bullivant G, Cordeiro D, Sinasac DS, Blaser S, Mercimek-Mahmutoglu S. A new patient with intermediate severe salla disease with hypomyelination: a literature review for Salla disease. Pediatr Neurol. 2017;74:87–91.e2. doi: 10.1016/j.pediatrneurol.2017.05.022. - DOI - PubMed
    1. Zielonka M, Garbade SF, Kölker S, Hoffmann GF, Ries M. A cross-sectional quantitative analysis of the natural history of free sialic acid storage disease—an ultra-orphan multisystemic lysosomal storage disorder. Genet Med. 2019;21:347–352. doi: 10.1038/s41436-018-0051-3. - DOI - PubMed

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