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3-Hydroxyacyl-CoA Dehydrogenase II Deficiency

3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: Introduction

3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay. More detailed information about the symptoms, causes, and treatments of 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency is available below.

Symptoms of 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency

Treatments for 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency

Wrongly Diagnosed with 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency?

3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: Complications

Review possible medical complications related to 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency:

Causes of 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency

More information about causes of 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency:

Misdiagnosis and 3-Hydroxyacyl-CoA Dehydrogenase II 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). See symptoms of Vitamin B12...read more »

3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: Broader Related Topics

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More information about 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency

  1. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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