The protracted form of juvenile neuronal ceroid-lipofuscinosis.
作者： Hans H. Goebel , Hartmut Pilz , Filippo Gullotta
DOI: 10.1007/BF00699645
关键词:
摘要: Clinical and ultrastructural findings consisting of curvilinear fingerprint residual bodies, in a protracted juvenile form NCL are reported from woman who died at the age 35 years. Homochrony homotypy her brother's illness emphasize intrafamilial similarities within subgroups lysosomal disorders.
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