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Article

Neuronal ceroid lipofuscinosis in the Czech Republic: analysis of 57 cases. Report of the 'Prague NCL group'.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society - 1 Jan 1997

Elleder M, Franc J, Kraus J, Nevsímalová S, Sixtová K, Zeman J

Abstract excerpt

A series of 57 patients (from 51 families) with neuronal ceroid lipofuscinosis (NCL) has been diagnosed during the last 25 years. Using clinical and electrophysiological criteria together with results of ultrastructural, histochemical, immunohistochemical and neuropathological analyses it has been possible to classify the following NCL types. Two cases were of the infantile type (CLN1), one case of the juvenile...

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Source

Identifiers

PMID: 10728204
DOI: 10.1016/s1090-3798(97)80041-4

Genes

CLN6
CLN3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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