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What is Triglyceride storage disease with impaired long-chain fatty acid oxidation?

What is Triglyceride storage disease with impaired long-chain fatty acid oxidation?

  • Triglyceride storage disease with impaired long-chain fatty acid oxidation: A rare inherited disorder involving the metabolism of fat which causes skin, muscle and blood abnormalities.

Triglyceride storage disease with impaired long-chain fatty acid oxidation is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Triglyceride storage disease with impaired long-chain fatty acid oxidation, or a subtype of Triglyceride storage disease with impaired long-chain fatty acid oxidation, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Triglyceride storage disease with impaired long-chain fatty acid oxidation: Introduction

Types of Triglyceride storage disease with impaired long-chain fatty acid oxidation:

Broader types of Triglyceride storage disease with impaired long-chain fatty acid oxidation:

How serious is Triglyceride storage disease with impaired long-chain fatty acid oxidation?

Complications of Triglyceride storage disease with impaired long-chain fatty acid oxidation: see complications of Triglyceride storage disease with impaired long-chain fatty acid oxidation

What causes Triglyceride storage disease with impaired long-chain fatty acid oxidation?

Causes of Triglyceride storage disease with impaired long-chain fatty acid oxidation: see causes of Triglyceride storage disease with impaired long-chain fatty acid oxidation

What are the symptoms of Triglyceride storage disease with impaired long-chain fatty acid oxidation?

Symptoms of Triglyceride storage disease with impaired long-chain fatty acid oxidation: see symptoms of Triglyceride storage disease with impaired long-chain fatty acid oxidation

Complications of Triglyceride storage disease with impaired long-chain fatty acid oxidation: see complications of Triglyceride storage disease with impaired long-chain fatty acid oxidation

Triglyceride storage disease with impaired long-chain fatty acid oxidation: Testing

Diagnostic testing: see tests for Triglyceride storage disease with impaired long-chain fatty acid oxidation.

Misdiagnosis: see misdiagnosis and Triglyceride storage disease with impaired long-chain fatty acid oxidation.

How is it treated?

Doctors and Medical Specialists for Triglyceride storage disease with impaired long-chain fatty acid oxidation: Medical Geneticist ; see also doctors and medical specialists for Triglyceride storage disease with impaired long-chain fatty acid oxidation.
Treatments for Triglyceride storage disease with impaired long-chain fatty acid oxidation: see treatments for Triglyceride storage disease with impaired long-chain fatty acid oxidation

Name and Aliases of Triglyceride storage disease with impaired long-chain fatty acid oxidation

Main name of condition: Triglyceride storage disease with impaired long-chain fatty acid oxidation

Other names or spellings for Triglyceride storage disease with impaired long-chain fatty acid oxidation:

ichthyosis, Chanarin Dorfman syndrome, Neutral lipid storage myopathy, Ichthyotic neutral lipid storage disease, Chanarin-Dorfman disease, Ichthyosiform erythroderma with leukocyte vacuolation, Dorfman Chanarin syndrome, DCS

Neutral lipid storage myopathy, Chanarin-Dorfman disease, DCS, Dorfman Chanarin syndrome, Ichthyosiform erythroderma with leukocyte vacuolation, Ichthyotic neutral lipid storage disease
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Triglyceride storage disease with impaired long-chain fatty acid oxidation: Related Conditions

Research the causes of these diseases that are similar to, or related to, Triglyceride storage disease with impaired long-chain fatty acid oxidation:

 

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