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
See full list of 13
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 of multiple sclerosis).
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Read more about Misdiagnosis and Phosphoserine aminotransferase deficiency
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.
More about prognosis of Phosphoserine aminotransferase deficiency
Phosphoserine aminotransferase deficiency: Broader Related Topics
Types of Phosphoserine aminotransferase deficiency
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