Abstract
3-Phosphoglycerate dehydrogenase (3-PGDH) deficiency is an inborn error of serine biosynthesis. Patients are affected with congenital microcephaly, psychomotor retardation, and intractable seizures. The effects of oral treatment with amino acids were investigated in 2 siblings. L-Serine up to 500 mg/kg/day was not sufficient for seizure control. Addition of glycine 200 mg/kg/day resulted in complete disappearance of seizures. Electroencephalographic abnormalities gradually resolved after 6 months. We conclude that 3-PGDH can be treated effectively by a combination of L-serine and glycine.
MeSH terms
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Carbohydrate Dehydrogenases / deficiency*
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Child
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Child, Preschool
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Drug Therapy, Combination
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Electroencephalography / drug effects
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Glycine / blood
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Glycine / cerebrospinal fluid
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Glycine / pharmacology
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Glycine / therapeutic use*
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Humans
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Infant, Newborn
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Intellectual Disability / etiology*
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Male
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Microcephaly / etiology*
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Phosphoglycerate Dehydrogenase
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Seizures / drug therapy*
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Seizures / enzymology
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Seizures / etiology
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Serine / blood
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Serine / cerebrospinal fluid
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Serine / pharmacology
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Serine / therapeutic use*
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Tetrahydrofolates / cerebrospinal fluid
Substances
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Tetrahydrofolates
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Serine
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Carbohydrate Dehydrogenases
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Phosphoglycerate Dehydrogenase
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Glycine
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5-methyltetrahydrofolate