- Case Report
- Two Cases of HHH Syndrome in Siblings
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Min Ho Hwang, Bo Sun Kim, Dong Hwan Lee
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Clin Exp Pediatr. 2001;44(10):1206-1210. Published online October 15, 2001
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Hyperornithinemia-hyperammonemia-homocitrullinuria(HHH) syndrome is a rare autosomal recessive disorder caused by a defect in the urea cycle. Protein intolerance, mental retardation, seizure, ataxia, and stupor are characteristic symptoms. Patients showing these symptoms may also present symptoms of acute hepatic disease at the same time. When fed with a high protein diet, they may refuse to eat, vomit, become lethargic, or go... |
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