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Corticosterone Methyloxidase type I Deficiency

Corticosterone Methyloxidase type I Deficiency: Introduction

Corticosterone Methyloxidase type I Deficiency: A very rare genetic disorder where deficiency of a particularly chemical (aldosterone synthase) results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated. More detailed information about the symptoms, causes, and treatments of Corticosterone Methyloxidase type I Deficiency is available below.

Symptoms of Corticosterone Methyloxidase type I Deficiency

Treatments for Corticosterone Methyloxidase type I Deficiency

Wrongly Diagnosed with Corticosterone Methyloxidase type I Deficiency?

Corticosterone Methyloxidase type I Deficiency: Related Patient Stories

Causes of Corticosterone Methyloxidase type I Deficiency

More information about causes of Corticosterone Methyloxidase type I Deficiency:

Misdiagnosis and Corticosterone Methyloxidase type I 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 »

Prognosis for Corticosterone Methyloxidase type I Deficiency

Prognosis for Corticosterone Methyloxidase type I Deficiency: Symptoms usually improve with age and adults may be completely asymptomatic. The biggest danger is during infancy where acute crises may result in death.

Corticosterone Methyloxidase type I Deficiency: Broader Related Topics

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More information about Corticosterone Methyloxidase type I Deficiency

  1. Corticosterone Methyloxidase type I Deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Prognosis
 

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