Wolfram syndrome: evidence of a diffuse neurodegenerative disease by magnetic resonance imaging
- PMID: 1603350
- DOI: 10.1212/wnl.42.6.1220
Wolfram syndrome: evidence of a diffuse neurodegenerative disease by magnetic resonance imaging
Abstract
Wolfram syndrome is an autosomal recessive disorder beginning in childhood that consists of four cardinal features: optic atrophy, diabetes mellitus, diabetes insipidus, and neurosensory hearing loss. Aside from these features, the clinical picture is highly variable and may include other neurologic abnormalities such as ataxia, nystagmus, mental retardation, and seizures. We present two unrelated patients with Wolfram syndrome, both of whom had the four cardinal features and several other neurologic abnormalities. MRIs showed widespread atrophic changes throughout the brain, some of which correlated with the major neurologic features of the syndrome.
Similar articles
-
Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy.Ann Neurol. 1996 Mar;39(3):352-60. doi: 10.1002/ana.410390312. Ann Neurol. 1996. PMID: 8602754
-
Primary diagnosis of Wolfram syndrome in an adult patient--case report and description of a novel pathogenic mutation.J Neurol Sci. 2011 Jan 15;300(1-2):191-3. doi: 10.1016/j.jns.2010.08.044. Epub 2010 Sep 28. J Neurol Sci. 2011. PMID: 20875904
-
Juvenile onset diabetes mellitus, central diabetes insipidus and optic atrophy (Wolfram syndrome)--neurological findings and prognostic implications.Neuropediatrics. 1991 May;22(2):103-6. doi: 10.1055/s-2008-1071426. Neuropediatrics. 1991. PMID: 1857494
-
Wolfram syndrome: case report and review of the literature.Compr Ther. 2007 Spring;33(1):18-20. doi: 10.1007/s12019-007-0007-z. Compr Ther. 2007. PMID: 17984488 Review.
-
Wolfram syndrome: case report and review of the literature.Ann Ophthalmol (Skokie). 2007 Spring;39(1):53-5. doi: 10.1007/BF02697327. Ann Ophthalmol (Skokie). 2007. PMID: 17914206 Review.
Cited by
-
Neuroimaging evidence of deficient axon myelination in Wolfram syndrome.Sci Rep. 2016 Feb 18;6:21167. doi: 10.1038/srep21167. Sci Rep. 2016. PMID: 26888576 Free PMC article. Clinical Trial.
-
Imaging of the brain in children with type I diabetes mellitus.Pediatr Radiol. 2007 Sep;37(9):863-9. doi: 10.1007/s00247-007-0536-8. Epub 2007 Jul 10. Pediatr Radiol. 2007. PMID: 17619872 Review.
-
Case Report: A novel mutation in WFS1 gene (c.1756G>A p.A586T) is responsible for early clinical features of cognitive impairment and recurrent ischemic stroke.Front Genet. 2023 Feb 2;14:1072978. doi: 10.3389/fgene.2023.1072978. eCollection 2023. Front Genet. 2023. PMID: 36816038 Free PMC article.
-
Wolfram (DIDMOAD) syndrome.J Med Genet. 1997 Oct;34(10):838-41. doi: 10.1136/jmg.34.10.838. J Med Genet. 1997. PMID: 9350817 Free PMC article. Review.
-
Expression and localization of Wolfram syndrome 1 gene in the developing rat pancreas.World J Gastroenterol. 2009 Nov 21;15(43):5425-31. doi: 10.3748/wjg.15.5425. World J Gastroenterol. 2009. PMID: 19916172 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical