CSF insulin-like growth factor-1 in infantile neuronal ceroid lipofuscinosis

Infantile neuronal ceroid lipofuscinosis (INCL) is a progressive encephalopathy in which the patients are severely disabled by the age of 3 years. It is characterized by cerebral atrophy, selective loss of cortical neurons, and secondary loss of axons and myelin sheaths of the white matter. INCL has...

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Veröffentlicht in:	Neurology 2000-05, Vol.54 (9), p.1828-1832
Hauptverfasser:	RIIKONEN, R, VANHANEN, S.-L, TYYNELÄ, J, SANTAVUORI, P, TURPEINEN, U
Format:	Artikel
Sprache:	eng
Schlagworte:	Apoptosis - physiology Biological and medical sciences Biopsy Child, Preschool Errors of metabolism Female Humans Infant Insulin-Like Growth Factor Binding Protein 3 - cerebrospinal fluid Insulin-Like Growth Factor I - cerebrospinal fluid Lipids (lysosomal enzyme disorders, storage diseases) Male Medical sciences Metabolic diseases Myelin Sheath - pathology Neuronal Ceroid-Lipofuscinoses - cerebrospinal fluid Neuronal Ceroid-Lipofuscinoses - diagnosis Neuronal Ceroid-Lipofuscinoses - pathology Neurons - pathology Radioimmunoassay
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