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What is Juvenile Megaloblastic Anemia?

What is Juvenile Megaloblastic Anemia?

  • Juvenile Megaloblastic Anemia: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.

Juvenile Megaloblastic Anemia: Introduction

Types of Juvenile Megaloblastic Anemia:

Broader types of Juvenile Megaloblastic Anemia:

Who gets Juvenile Megaloblastic Anemia?

Racial predominance for Juvenile Megaloblastic Anemia: Most cases have been diagnosed in Eastern Mediterranean countries.

How serious is Juvenile Megaloblastic Anemia?

Complications of Juvenile Megaloblastic Anemia: see complications of Juvenile Megaloblastic Anemia

What causes Juvenile Megaloblastic Anemia?

Causes of Juvenile Megaloblastic Anemia: see causes of Juvenile Megaloblastic Anemia
Cause of Juvenile Megaloblastic Anemia: The condition originates from a genetic defect which is inherited in an autosomal recessive manner.

What are the symptoms of Juvenile Megaloblastic Anemia?

Symptoms of Juvenile Megaloblastic Anemia: see symptoms of Juvenile Megaloblastic Anemia

Complications of Juvenile Megaloblastic Anemia: see complications of Juvenile Megaloblastic Anemia

Onset of Juvenile Megaloblastic Anemia: Symptoms can develop from months to years after birth but usually occurs during the 2nd year of life.

Can anyone else get Juvenile Megaloblastic Anemia?

Inheritance: see inheritance of Juvenile Megaloblastic Anemia

Juvenile Megaloblastic Anemia: Testing

Diagnostic testing: see tests for Juvenile Megaloblastic Anemia.

Misdiagnosis: see misdiagnosis and Juvenile Megaloblastic Anemia.

How is it treated?

Treatments for Juvenile Megaloblastic Anemia: see treatments for Juvenile Megaloblastic Anemia

Name of Juvenile Megaloblastic Anemia

Main name of condition: Juvenile Megaloblastic Anemia

 

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