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Neuronal Ceroid-Lipofuscinosis
Description:
An illustrated transverse section of the brain of a patient suffering from neuronal ceroid lipofuscinosis (NCL). This inherited neurological disorder appears during infancy and is characterized based on the age of disease onset. Genetic mutations prevent proteins from being broken down and accumulate into fatty substances known as lipopigments. The brain begins to atrophy during progressive death of brain cells, with affected brains displaying enlarged sulci and dilated ventricles, along with periventricular white matter lesions.
Credit:
Evan Oto/Science Source
Unique identifier:
SS2712743
Legacy Identifier:
JC7423
Type:
Image
Size:
2550px × 3300px (~24 MB)
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Tags
anatomy
annotated
art
batten disease
brain
cln disease
diagram
illustration
incl
infantile neuronal ceroid lipofuscinosis
information graphic
jncl
juvenile neuronal ceroid lipofuscinosis
labeled
late infantile neuronal ceroid lipofuscinosis
lincl
lysosome
medical illustration
ncl
neurological disorder
neuronal ceroid lipofuscinosis
