About The Medical Condition Hyperlysinemia, Familial
Find the definition of the medical term Hyperlysinemia, Familial. Hyperlysinemia, Familial defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Hyperlysinemia, Familial
| Hyperlysinemia, Familial Medical Condition |
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What's The Definition Of The Medical Condition Hyperlysinemia, Familial?
A group of inherited metabolic disorders which have in common elevations of serum LYSINE levels. Enzyme deficiencies of alpha-aminoadipic semialdehyde dehydrogenase and the SACCHAROPINE DEHYDROGENASES have been associated with hyperlysinemia. Clinical manifestations include mental retardation, recurrent emesis, hypotonia, lethargy, diarrhea, and developmental delay. (From Menkes, Textbook of Child Neurology, 5th ed, p56)
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