The protracted form of juvenile neuronal ceroid-lipofuscinosis

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 1976 English Publisher:Springer Science and Business Media LLCJournal:Acta Neuropathologica, volume 36, pages 393-396 (issn: 0001-6322, eissn: 1432-0533,

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Authors: H H, Goebel; H, Pilz; F, Gullotta;

doi: 10.1007/bf00699645

pmid: 189559

The protracted form of juvenile neuronal ceroid-lipofuscinosis

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Abstract

Clinical and ultrastructural findings consisting of curvilinear and fingerprint residual bodies, in a protracted juvenile form of NCL are reported from a woman who died at the age of 35 years. Homochrony and homotypy of her brother's illness emphasize intrafamilial similarities within subgroups of lysosomal disorders.

Related Organizations

University of Göttingen
Germany
University of Bonn
Germany

Keywords

Adult, Inclusion Bodies, Microscopy, Electron, Age Factors, Brain, Humans, Female, Lipidoses

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