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SCHAD Deficiency -- formerly

SCHAD Deficiency -- formerly: Introduction

SCHAD Deficiency -- formerly: A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activity prevents some fats being converted into energy. Symptoms tend to be exacerbated during fasting as during fasting, the body tries to rely more heavily on fats for energy. Fatty acids that are not completely metabolized due to the enzyme deficiency may build up in various organs and cause serious complications. More detailed information about the symptoms, causes, and treatments of SCHAD Deficiency -- formerly is available below.

Symptoms of SCHAD Deficiency -- formerly

Wrongly Diagnosed with SCHAD Deficiency -- formerly?

SCHAD Deficiency -- formerly: Complications

Review possible medical complications related to SCHAD Deficiency -- formerly:

Causes of SCHAD Deficiency -- formerly

More information about causes of SCHAD Deficiency -- formerly:

Misdiagnosis and SCHAD Deficiency -- formerly

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See more »

SCHAD Deficiency -- formerly: Broader Related Topics

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More information about SCHAD Deficiency -- formerly

  1. SCHAD Deficiency -- formerly: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications

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