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Hyperdibasic aminoaciduria type 2

Hyperdibasic aminoaciduria type 2: Introduction

Hyperdibasic aminoaciduria type 2: A rare inborn urea cycle disorder characterized by an enzyme defect in the amino acid transporter gene SLC7A7 (positive amino acid transporter). More detailed information about the symptoms, causes, and treatments of Hyperdibasic aminoaciduria type 2 is available below.

Symptoms of Hyperdibasic aminoaciduria type 2

Treatments for Hyperdibasic aminoaciduria type 2

  • Treatment involves reducing protein in the diet and using lysine, ornithin and citrulline supplements
  • more treatments...»

Home Diagnostic Testing

Home medical testing related to Hyperdibasic aminoaciduria type 2:

Wrongly Diagnosed with Hyperdibasic aminoaciduria type 2?

Hyperdibasic aminoaciduria type 2: Complications

Review possible medical complications related to Hyperdibasic aminoaciduria type 2:

Causes of Hyperdibasic aminoaciduria type 2

  • The genetic disorder is inherited in an autosomal recessive manner
  • more causes...»

More information about causes of Hyperdibasic aminoaciduria type 2:

Less Common Symptoms of Hyperdibasic aminoaciduria type 2

Hyperdibasic aminoaciduria type 2: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Hyperdibasic aminoaciduria type 2

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Hyperdibasic aminoaciduria type 2: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Prognosis for Hyperdibasic aminoaciduria type 2

Prognosis for Hyperdibasic aminoaciduria type 2: The prognosis is variable depending on how well the condition is managed and whether lung complications develop.

Hyperdibasic aminoaciduria type 2: Broader Related Topics

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More information about Hyperdibasic aminoaciduria type 2

  1. Hyperdibasic aminoaciduria type 2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
  8. Prognosis
 

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