Phenotypic variability among adult siblings with Sjögren-Larsson syndrome

Alexander Lossos, Moona Khoury, William B Rizzo, John M. Gomori, Eyal Banin, Abraham Zlotogorski, Saleh Jaber, Oded Abramsky, Zohar Argov, Hanna Rosenmann

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Background: Sjögren-Larsson syndrome (SLS) is an early childhood-onset disorder with ichthyosis, mental retardation, spastic paraparesis, macular dystrophy, and leukoencephalopathy caused by the deficiency of fatty aldehyde dehydrogenase due to mutations in the ALDH3A2 gene (the gene that encodes microsomal fatty aldehyde dehydrogenase). Cerebral proton magnetic resonance spectroscopy in those with SLS demonstrates an abnormal white matter peak at 1.3 ppm, consistent with long-chain fatty alcohol accumulation. Objective: To define the clinical course and proton magnetic resonance spectroscopic findings of SLS in adults. Design and Setting: Case series in a tertiary care center. Patients: Six siblings of a consanguineous Arab family with early childhood-onset SLS who carry the 682C→T mutation in the ALDH3A2 gene were reinvestigated in adulthood. Results: The 6 affected siblings ranged in age from 16 to 36 years. All exhibited the typical clinical and imaging manifestations of SLS, but their severity markedly varied. Neurological involvement was apparently nonprogressive, and its severity showed no correlation with age. Cerebral proton magnetic resonance spectroscopy showed a lipid peak at 1.3 ppm, with decreasing intensity in the older siblings. Conclusion: These observations document significant clinical variability and the nonprogressive neurological course of SLS in adult siblings with the same ALDH3A2 genotype, and demonstrate possible correlation of proton magnetic resonance spectroscopic changes with age, suggesting unknown pathogenic mechanisms to compensate for the responsible biochemical defect in this disease.

Original languageEnglish (US)
Pages (from-to)278-280
Number of pages3
JournalArchives of Neurology
Volume63
Issue number2
DOIs
StatePublished - Feb 1 2006

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Siblings
long-chain-aldehyde dehydrogenase
Protons
Sjogren-Larsson Syndrome
Magnetic Resonance Spectroscopy
Spastic Paraparesis
Fatty Alcohols
Genes
Ichthyosis
Leukoencephalopathies
Mutation
Macular Degeneration
Tertiary Care Centers
Intellectual Disability
Syndrome
Genotype
Lipids
Gene
Proton Magnetic Resonance Spectroscopy
Spectroscopy

ASJC Scopus subject areas

  • Arts and Humanities (miscellaneous)
  • Clinical Neurology

Cite this

Lossos, A., Khoury, M., Rizzo, W. B., Gomori, J. M., Banin, E., Zlotogorski, A., ... Rosenmann, H. (2006). Phenotypic variability among adult siblings with Sjögren-Larsson syndrome. Archives of Neurology, 63(2), 278-280. https://doi.org/10.1001/archneur.63.2.278

Phenotypic variability among adult siblings with Sjögren-Larsson syndrome. / Lossos, Alexander; Khoury, Moona; Rizzo, William B; Gomori, John M.; Banin, Eyal; Zlotogorski, Abraham; Jaber, Saleh; Abramsky, Oded; Argov, Zohar; Rosenmann, Hanna.

In: Archives of Neurology, Vol. 63, No. 2, 01.02.2006, p. 278-280.

Research output: Contribution to journalArticle

Lossos, A, Khoury, M, Rizzo, WB, Gomori, JM, Banin, E, Zlotogorski, A, Jaber, S, Abramsky, O, Argov, Z & Rosenmann, H 2006, 'Phenotypic variability among adult siblings with Sjögren-Larsson syndrome', Archives of Neurology, vol. 63, no. 2, pp. 278-280. https://doi.org/10.1001/archneur.63.2.278
Lossos, Alexander ; Khoury, Moona ; Rizzo, William B ; Gomori, John M. ; Banin, Eyal ; Zlotogorski, Abraham ; Jaber, Saleh ; Abramsky, Oded ; Argov, Zohar ; Rosenmann, Hanna. / Phenotypic variability among adult siblings with Sjögren-Larsson syndrome. In: Archives of Neurology. 2006 ; Vol. 63, No. 2. pp. 278-280.
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