A variant of Jansky-Bielschowsky disease
- PMID: 7133332
- DOI: 10.1055/s-2008-1059612
A variant of Jansky-Bielschowsky disease
Abstract
A series of 18 patients with Jansky-Bielschowsky disease is presented. Two children only showed the classical features of the disorder, whereas the remaining 16 differed from the cases previously published in the following respects. Clinically: later onset of age, early onset of visual failure and an intermediate course of the disease. Neurophysiologically: spikes in response to intermittent stimulation appeared by the age of 7-8 years and disappeared after 11 years. The visual evoked response was extinct at an advanced stage of the disorder. Morphologically: accumulation of cytosomes with curvi-linear and fingerprint profiles in solid tissues, but lymphocytes showed no storage material. Electron microscopy of the lymphocytes revealed nothing abnormal.
Similar articles
-
The spectrum of Jansky-Bielschowsky disease.Neuropediatrics. 1991 May;22(2):92-6. doi: 10.1055/s-2008-1071423. Neuropediatrics. 1991. PMID: 1649978
-
Neurophysiological findings in neuronal ceroid lipofuscinoses.Neuropediatrics. 1997 Feb;28(1):70. doi: 10.1055/s-2007-973673. Neuropediatrics. 1997. PMID: 9151328 No abstract available.
-
Childhood neuronal ceroid-lipofuscinoses in Argentina.Am J Med Genet. 1995 Jun 5;57(2):144-9. doi: 10.1002/ajmg.1320570207. Am J Med Genet. 1995. PMID: 7668319
-
[Jansky-Bielschowsky disease].Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):252-4. Ryoikibetsu Shokogun Shirizu. 2002. PMID: 12483874 Review. Japanese. No abstract available.
-
Early juvenile neuronal ceroid-lipofuscinosis or variant Jansky-Bielschowsky disease: diagnostic criteria and nomenclature.J Inherit Metab Dis. 1993;16(2):230-2. doi: 10.1007/BF00710251. J Inherit Metab Dis. 1993. PMID: 8411967 Review. No abstract available.
Cited by
-
MRI of neuronal ceroid lipofuscinosis. I. Cranial MRI of 30 patients with juvenile neuronal ceroid lipofuscinosis.Neuroradiology. 1996 Jul;38(5):476-82. doi: 10.1007/BF00607283. Neuroradiology. 1996. PMID: 8837098
-
Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses.Am J Hum Genet. 1994 Oct;55(4):695-701. Am J Hum Genet. 1994. PMID: 7942847 Free PMC article.
-
Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16.Am J Hum Genet. 1993 Jan;52(1):89-95. Am J Hum Genet. 1993. PMID: 8434611 Free PMC article.
-
The neuronal ceroid-lipofuscinoses (Batten disease): a new class of lysosomal storage diseases.J Inherit Metab Dis. 1999 Jun;22(4):535-44. doi: 10.1023/a:1005564509027. J Inherit Metab Dis. 1999. PMID: 10407785 Review.
-
Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCL.Neurobiol Dis. 2009 May;34(2):308-19. doi: 10.1016/j.nbd.2009.02.001. Neurobiol Dis. 2009. PMID: 19385065 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources