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
See full list of 18
symptoms of Corticosterone Methyloxidase type I Deficiency
Treatments for Corticosterone Methyloxidase type I Deficiency
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Wrongly Diagnosed with Corticosterone Methyloxidase type I Deficiency?
Corticosterone Methyloxidase type I Deficiency: Related Patient Stories
Causes of Corticosterone Methyloxidase type I Deficiency
- The condition is inherited in an autosomal recessive manner
- more causes...»
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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 ...read more »
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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.
More about prognosis of Corticosterone Methyloxidase type I Deficiency
Corticosterone Methyloxidase type I Deficiency: Broader Related Topics
Types of Corticosterone Methyloxidase type I Deficiency
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