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Phosphoserine aminotransferase deficiency

Phosphoserine aminotransferase deficiency: Introduction

Phosphoserine aminotransferase deficiency: A recessively inherited enzyme (phosphoserine aminotransferase) deficiency which manifests as uncontrollable seizures, psychomotor retardation, small head and increased muscle tone. Treatment from birth can prevent early death and allow a relatively normal life. More detailed information about the symptoms, causes, and treatments of Phosphoserine aminotransferase deficiency is available below.

Symptoms of Phosphoserine aminotransferase deficiency

Wrongly Diagnosed with Phosphoserine aminotransferase deficiency?

Phosphoserine aminotransferase deficiency: Complications

Review possible medical complications related to Phosphoserine aminotransferase deficiency:

Causes of Phosphoserine aminotransferase deficiency

Read more about causes of Phosphoserine aminotransferase deficiency.

Misdiagnosis and Phosphoserine aminotransferase 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...read more »

Prognosis for Phosphoserine aminotransferase deficiency

Prognosis for Phosphoserine aminotransferase deficiency: Early death occurs without treatment. Treatment needs to be started soon after birth and involves administration of serine and glycine.

Phosphoserine aminotransferase deficiency: Broader Related Topics

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More information about Phosphoserine aminotransferase deficiency

  1. Phosphoserine aminotransferase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
  7. Prognosis
 

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