Literature DB >> 650259

Early-juvenile Batten's disease--a recognisable sub-group distinct from other forms of Batten's disease. Analysis of 5 patients.

B D Lake, N P Cavanagh.   

Abstract

In most cases where rectal biopsy is performed to diagnose Batten's disease, there is good correlation between biopsy appearance, age of onset, clinical course and electrophysiological parameters. As a result 3 forms of the disease have been recognised; infantile, late infantile and juvenile. In a review of rectal biopsy in Batten's disease at the Hospital for Sick Children, Great Ormond Street, we have studied the few cases in which no such correlation appeared to exist. In 5 the features are sufficiently similar to suggest a further recognisable sub-group which could be descriptively called "early juvenile". The clinical course, electrophysiological features and the absence of vacuolated lymphocytes in this subgroup are as found in the late infantile form, whereas the biopsy findings are identical to those of the juvenile form. By analogy with some of the mucopolysaccharidoses we speculate that the genes of the late infantile and juvenile forms of Batten's disease are allelic and that the "early juvenile" sub-group is a genetic compound presenting as an intermediate phenotype.

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Year:  1978        PMID: 650259     DOI: 10.1016/0022-510x(78)90087-4

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  15 in total

Review 1.  Neuronal ceroid lipofuscinoses: a review.

Authors:  N Nardocci; F Cardona
Journal:  Ital J Neurol Sci       Date:  1998-10

Review 2.  Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses.

Authors:  Sara E Mole; Ruth E Williams; Hans H Goebel
Journal:  Neurogenetics       Date:  2005-09-28       Impact factor: 2.660

3.  Blood lymphocytes in neuronal ceroid lipofuscinosis.

Authors:  A Simonati; N Rizzuto
Journal:  Ital J Neurol Sci       Date:  1988-06

4.  Electrophysiological findings of neuronal ceroid lipofuscinosis in heterozygotes.

Authors:  I Gottlob; K P Leipert; A Kohlschütter; H H Goebel
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1988       Impact factor: 3.117

5.  Adult ceroid-lipofuscinosis: diagnostic value of biopsies and of neurophysiological investigations.

Authors:  A Vercruyssen; J J Martin; C Ceuterick; K Jacobs; L Swerts
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-11       Impact factor: 10.154

6.  Dolichol metabolism in cultured skin fibroblasts from patients with "neuronal" ceroid lipofuscinosis (Batten's disease).

Authors:  B C Paton; A Poulos
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

7.  Autofluorescence emission spectra of neuronal lipopigment in animal and human ceroidoses (ceroid-lipofuscinoses).

Authors:  J H Dowson; D Armstrong; N Koppang; B D Lake; R D Jolly
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

8.  Protein product of CLN6 gene responsible for variant late-onset infantile neuronal ceroid lipofuscinosis interacts with CRMP-2.

Authors:  Jared W Benedict; Amanda L Getty; Thomas M Wishart; Thomas H Gillingwater; David A Pearce
Journal:  J Neurosci Res       Date:  2009-07       Impact factor: 4.164

9.  Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes.

Authors:  R Williams; J Vesa; I Järvelä; T McKay; H Mitchison; E Hellsten; A Thompson; D Callen; G Sutherland; D Luna-Battadano
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

10.  A dominant form of neuronal ceroid-lipofuscinosis. An ultrastructural study of sural nerve and peripheral lymphocytes.

Authors:  B Badurska; A Fidziańska; H Jedrzejowska
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

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