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Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

Deficiency of Member 8 Acyl-CoA Dehydrogenace Family: Introduction

Deficiency of Member 8 Acyl-CoA Dehydrogenace Family: An extremely rare metabolic disorder where the body is unable to metabolize certain proteins properly. More specifically, an insufficient level of the enzyme (isobutyryl-coenzyme A dehydrogenase) needed to metabolize the amino acid valine. The onset and severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Deficiency of Member 8 Acyl-CoA Dehydrogenace Family is available below.

Symptoms of Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

Treatments for Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

Wrongly Diagnosed with Deficiency of Member 8 Acyl-CoA Dehydrogenace Family?

Deficiency of Member 8 Acyl-CoA Dehydrogenace Family: Complications

Review possible medical complications related to Deficiency of Member 8 Acyl-CoA Dehydrogenace Family:

  • Frequent vomiting
  • Dehydration due to vomiting
  • Worsening of symptoms during fasting
  • Worsening of symptoms due to infection
  • more complications...»

Causes of Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

  • The condition is a genetic anomaly inherited in an autosomal recessive manner
  • more causes...»

More information about causes of Deficiency of Member 8 Acyl-CoA Dehydrogenace Family:

Misdiagnosis and Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

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...read more »

Prognosis for Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

Prognosis for Deficiency of Member 8 Acyl-CoA Dehydrogenace Family: Early diagnosis and treatment can significantly improve the prognosis.

Deficiency of Member 8 Acyl-CoA Dehydrogenace Family: Broader Related Topics

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More information about Deficiency of Member 8 Acyl-CoA Dehydrogenace Family

  1. Deficiency of Member 8 Acyl-CoA Dehydrogenace Family: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
  7. Prognosis
 

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