Hyperprolinemia

Hyperprolinemia is a condition characterized by elevated levels of a particular amino acid called proline in the blood. This condition can occur in two forms, known as type I and type II.

Type I Hyperprolinemia

Type I hyperprolinemia is the milder form of the condition. It is often detected during newborn screening or during family studies following the diagnosis of a sibling. Most individuals with type I hyperprolinemia are asymptomatic and have normal growth and development.

Type II Hyperprolinemia

Type II hyperprolinemia is a more severe form of the condition. It is associated with intellectual disability and seizures.

Causes

Hyperprolinemia is caused by mutations in the PRODH gene (type I) or the ALDH4A1 gene (type II). These genes provide instructions for making enzymes that are involved in the breakdown of the amino acid proline.

Diagnosis

Hyperprolinemia is diagnosed based on the symptoms, clinical exam, and confirmed by laboratory testing showing elevated levels of proline in the blood.

Treatment

There is no specific treatment for hyperprolinemia. Management is supportive and depends on the symptoms in each individual.

See Also

• Amino acid
• PRODH
• ALDH4A1

References

• Genetics Home Reference. Hyperprolinemia. Available at: https://ghr.nlm.nih.gov/condition/hyperprolinemia
• National Organization for Rare Disorders. Hyperprolinemia Type I. Available at: https://rarediseases.org/rare-diseases/hyperprolinemia-type-i/

Hyperprolinemia Resources
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