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Diseases » ACAD9 deficiency » Summary
 

What is ACAD9 deficiency?

What is ACAD9 deficiency?

  • ACAD9 deficiency: A metabolic disorder involving a deficiency of an enzyme (acyl-CoA dehydrogenase-9). The symptoms are variable and are usually triggered by a viral infection or ingestion of aspirin which can trigger a Reye-like episode which can cause death.

ACAD9 deficiency: Introduction

Types of ACAD9 deficiency:

Broader types of ACAD9 deficiency:

How serious is ACAD9 deficiency?

Prognosis of ACAD9 deficiency: The severity of the condition is variable with some patients dying from Cardiomyopathy during the first five years of life whereas other patients can live longer. A viral illness and ingestion of aspirin can lead to death.
Complications of ACAD9 deficiency: see complications of ACAD9 deficiency

What causes ACAD9 deficiency?

Causes of ACAD9 deficiency: see causes of ACAD9 deficiency

What are the symptoms of ACAD9 deficiency?

Symptoms of ACAD9 deficiency: see symptoms of ACAD9 deficiency

Complications of ACAD9 deficiency: see complications of ACAD9 deficiency

ACAD9 deficiency: Testing

Misdiagnosis: see misdiagnosis and ACAD9 deficiency.

How is it treated?

Doctors and Medical Specialists for ACAD9 deficiency: Medical Geneticist ; see also doctors and medical specialists for ACAD9 deficiency.
Treatments for ACAD9 deficiency: see treatments for ACAD9 deficiency

Name and Aliases of ACAD9 deficiency

Main name of condition: ACAD9 deficiency

Other names or spellings for ACAD9 deficiency:

deficiency of Acyl-CoA dehydrogenase family, member 9

 

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