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Health Dictionary

Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.

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Hyperlysinemia

Introduction


Hyperlysinemia is an autosomal recessive[1] metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It can be associated with saccharopine dehydrogenase.

Hyperlysinemia has an autosomal recessive pattern of inheritance.
See also

See also

References

References

  1. ↑ Sacksteder KA, Bier BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT (2000). “Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia”. American journal of human genetics. 66 (6): 1736–1743. doi:10.1086/302919. PMC 1378037. PMID 10775527. Unknown parameter |month= ignored (help)