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LADHSC deficiency

LADHSC deficiency: Introduction

LADHSC 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 LADHSC deficiency is available below.

Symptoms of LADHSC deficiency

Wrongly Diagnosed with LADHSC deficiency?

LADHSC deficiency: Complications

Review possible medical complications related to LADHSC deficiency:

Causes of LADHSC deficiency

More information about causes of LADHSC deficiency:

Misdiagnosis and LADHSC deficiency

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

LADHSC deficiency: Broader Related Topics

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More information about LADHSC deficiency

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

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