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Homocystinuria due to defect in methylation (cbl g)

Homocystinuria due to defect in methylation (cbl g): Introduction

Homocystinuria due to defect in methylation (cbl g): An inherited organic acid disorder where an enzyme deficiency (methionine synthase) impairs the body's ability to break down certain proteins consumed in the diet. This results in a buildup of methylmalonic acid and homocystine which results in harmful affects. It is a form of vitamin B12 deficiency. More detailed information about the symptoms, causes, and treatments of Homocystinuria due to defect in methylation (cbl g) is available below.

Symptoms of Homocystinuria due to defect in methylation (cbl g)

Home Diagnostic Testing

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Wrongly Diagnosed with Homocystinuria due to defect in methylation (cbl g)?

Causes of Homocystinuria due to defect in methylation (cbl g)

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Homocystinuria due to defect in methylation (cbl g): Undiagnosed Conditions

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Misdiagnosis and Homocystinuria due to defect in methylation (cbl g)

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Homocystinuria due to defect in methylation (cbl g): Research Doctors & Specialists

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Prognosis for Homocystinuria due to defect in methylation (cbl g)

Prognosis for Homocystinuria due to defect in methylation (cbl g): early treatment is necessary to prevent permanent neurological damage

Homocystinuria due to defect in methylation (cbl g): Broader Related Topics

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More information about Homocystinuria due to defect in methylation (cbl g)

  1. Homocystinuria due to defect in methylation (cbl g): Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis
 

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