Paediatric Guidelines

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H



HMG CoA Synthase Deficiency (HMGCS Deficiency, HMGCS2, 3-methyl-3-hydroxyglutaryl CoA synthase deficiency)

Hyperammonaemia due to transport defects (Lysinuric protein intolerance, LPI, hyperornithinaemia, hyperammonaemia, homocitrullinuria, HHH syndrome)