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What is Ceroid lipofuscinosis, neuronal 2, late infantile type?

What is Ceroid lipofuscinosis, neuronal 2, late infantile type?

  • Ceroid lipofuscinosis, neuronal 2, late infantile type: A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (protease tri-peptidyl-peptidase) needed to process it.

Ceroid lipofuscinosis, neuronal 2, late infantile type 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 2, late infantile type, or a subtype of Ceroid lipofuscinosis, neuronal 2, late infantile type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ceroid lipofuscinosis, neuronal 2, late infantile type: Introduction

Types of Ceroid lipofuscinosis, neuronal 2, late infantile type:

Broader types of Ceroid lipofuscinosis, neuronal 2, late infantile type:

How serious is Ceroid lipofuscinosis, neuronal 2, late infantile type?

Complications of Ceroid lipofuscinosis, neuronal 2, late infantile type: see complications of Ceroid lipofuscinosis, neuronal 2, late infantile type

What causes Ceroid lipofuscinosis, neuronal 2, late infantile type?

Causes of Ceroid lipofuscinosis, neuronal 2, late infantile type: see causes of Ceroid lipofuscinosis, neuronal 2, late infantile type

What are the symptoms of Ceroid lipofuscinosis, neuronal 2, late infantile type?

Symptoms of Ceroid lipofuscinosis, neuronal 2, late infantile type: see symptoms of Ceroid lipofuscinosis, neuronal 2, late infantile type

Complications of Ceroid lipofuscinosis, neuronal 2, late infantile type: see complications of Ceroid lipofuscinosis, neuronal 2, late infantile type

Can anyone else get Ceroid lipofuscinosis, neuronal 2, late infantile type?

More information: see contagiousness of Ceroid lipofuscinosis, neuronal 2, late infantile type
Inheritance: see inheritance of Ceroid lipofuscinosis, neuronal 2, late infantile type

Ceroid lipofuscinosis, neuronal 2, late infantile type: Testing

Diagnostic testing: see tests for Ceroid lipofuscinosis, neuronal 2, late infantile type.

Misdiagnosis: see misdiagnosis and Ceroid lipofuscinosis, neuronal 2, late infantile type.

How is it treated?

Doctors and Medical Specialists for Ceroid lipofuscinosis, neuronal 2, late infantile type: Medical Geneticist ; see also doctors and medical specialists for Ceroid lipofuscinosis, neuronal 2, late infantile type.
Treatments for Ceroid lipofuscinosis, neuronal 2, late infantile type: see treatments for Ceroid lipofuscinosis, neuronal 2, late infantile type

Name and Aliases of Ceroid lipofuscinosis, neuronal 2, late infantile type

Main name of condition: Ceroid lipofuscinosis, neuronal 2, late infantile type

Other names or spellings for Ceroid lipofuscinosis, neuronal 2, late infantile type:

Jansky-Bielschowsky disease, CLN2, Neuronal ceroid lipofuscinosis, late infantile type, LINCL, Amaurotic idiocy, late infantile type

Amaurotic idiocy, late infantile type, CLN2, Jansky-Bielschowsky disease, LINCL, Neuronal ceroid lipofuscinosis, late infantile type
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Ceroid lipofuscinosis, neuronal 2, late infantile type: Related Conditions

Research the causes of these diseases that are similar to, or related to, Ceroid lipofuscinosis, neuronal 2, late infantile type:

 

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