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HADH deficiency

HADH deficiency: Introduction

HADH deficiency: 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 HADH deficiency is available below.

Symptoms of HADH deficiency

Wrongly Diagnosed with HADH deficiency?

HADH deficiency: Complications

Review possible medical complications related to HADH deficiency:

Causes of HADH deficiency

More information about causes of HADH deficiency:

Misdiagnosis and HADH deficiency

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

HADH deficiency: Broader Related Topics

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More information about HADH deficiency

  1. HADH deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications

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