The clinical symptoms are related to hyperammonemia and resemble those of other urea cycle diseases.
Etiology
The hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is caused by mutation in the SLC25A15 gene (MIM.603861).
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The clinical symptoms are related to hyperammonemia and resemble those of other urea cycle diseases.
Etiology
The hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is caused by mutation in the SLC25A15 gene (MIM.603861).