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HMG CoA synthetase deficiency

HMG CoA synthetase deficiency: Introduction

HMG CoA synthetase deficiency: An inherited metabolic defect due to the deficiency of an enzyme (HMG CoA synthetase) needed to form ketone bodies. Symptoms are often preceded by periods of fasting or illness. More detailed information about the symptoms, causes, and treatments of HMG CoA synthetase deficiency is available below.

Symptoms of HMG CoA synthetase deficiency

Wrongly Diagnosed with HMG CoA synthetase deficiency?

Causes of HMG CoA synthetase deficiency

Read more about causes of HMG CoA synthetase deficiency.

Misdiagnosis and HMG CoA synthetase deficiency

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...read more »

HMG CoA synthetase deficiency: Broader Related Topics

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More information about HMG CoA synthetase deficiency

  1. HMG CoA synthetase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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