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Mitochondrial trifunctional protein deficiency

Mitochondrial trifunctional protein deficiency: Introduction

Mitochondrial trifunctional protein deficiency: A rare genetic condition where the body is unable to convert certain fats to energy. More specifically, there is insufficient levels of a particular enzyme needed to metabolize a type of fat called long-chain fatty acids. More detailed information about the symptoms, causes, and treatments of Mitochondrial trifunctional protein deficiency is available below.

Symptoms of Mitochondrial trifunctional protein deficiency

Wrongly Diagnosed with Mitochondrial trifunctional protein deficiency?

Mitochondrial trifunctional protein deficiency: Complications

Review possible medical complications related to Mitochondrial trifunctional protein deficiency:

Causes of Mitochondrial trifunctional protein deficiency

Read more about causes of Mitochondrial trifunctional protein deficiency.

Disease Topics Related To Mitochondrial trifunctional protein deficiency

Research the causes of these diseases that are similar to, or related to, Mitochondrial trifunctional protein deficiency:

Misdiagnosis and Mitochondrial trifunctional protein deficiency

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as ...read more »

Statistics for Mitochondrial trifunctional protein deficiency

Mitochondrial trifunctional protein deficiency: Broader Related Topics

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Definitions of Mitochondrial trifunctional protein deficiency:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Mitochondrial trifunctional protein deficiency as a "rare disease".
Source - Orphanet

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More information about Mitochondrial trifunctional protein deficiency

  1. Mitochondrial trifunctional protein deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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