About The Medical Condition Familial Hyperlysinemias
Find the definition of the medical term Familial Hyperlysinemias. Familial Hyperlysinemias defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Familial Hyperlysinemias
| Familial Hyperlysinemias Medical Condition |
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What's The Definition Of The Medical Condition Familial Hyperlysinemias?
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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