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Ceroid lipofuscinosis, neuronal 4

Ceroid lipofuscinosis, neuronal 4: Introduction

Ceroid lipofuscinosis, neuronal 4: A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (palmitoyl-protein thioesterase 1) needed to process it. More detailed information about the symptoms, causes, and treatments of Ceroid lipofuscinosis, neuronal 4 is available below.

Symptoms of Ceroid lipofuscinosis, neuronal 4

See full list of 10 symptoms of Ceroid lipofuscinosis, neuronal 4

Ceroid lipofuscinosis, neuronal 4: Complications

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Disease Topics Related To Ceroid lipofuscinosis, neuronal 4

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Definitions of Ceroid lipofuscinosis, neuronal 4:

Ceroid lipofuscinosis, neuronal 4 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Ceroid lipofuscinosis, neuronal 4, or a subtype of Ceroid lipofuscinosis, neuronal 4, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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