UCDs are rare inherited metabolic disorders, and HHH syndrome accounts for only 1-3.8% of the reported UCDs [12, 13]. The acute manifestations of HHH syndrome include encephalopathy, altered levels of consciousness, and seizures, with some…
Liver transplantation can prevent the progression of neurological damage in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome and maintain long-term metabolic stability — The largest single-center experience | Orphanet Journal of Rare Diseases
