1.8.b

Disorders of lipoic acid and iron-sulfur metabolism

  • Lipoyltransferase 2 deficiency (Neonatal severe encephalopathy with lactic acidosis and brain abnormalities – NELABA)
  • Lipoic acid synthase deficiency (Hyperglycinemia, lactic acidosis, and seizures)
  • Lipoyltransferase 1 deficiency
  • NFU1 deficiency (Multiple mitochondrial dysfunctions syndrome type 1)
  • BOLA3 deficiency (Multiple mitochondrial dysfunctions syndrome type 2 with hyperglycinemia)
  • Glutaredoxin 5 deficiency
  • IBA57 deficiency
  • ISCA1 deficiency (Multiple mitochondrial dysfunctions syndrome type 5)
  • ISCA2 deficiency (Multiple mitochondrial dysfunctions syndrome type 4)
  • ISCU deficiency (Hereditary myopathy with lactic acidosis, Swedish type myopathy with exercise intolerance)
  • ABCB7 deficiency (Sideroblastic anemia and spinocerebellar ataxia)
  • Ferredoxin reductase deficiency (Auditory neuropathy and optic atrophy)
  • Ferredoxin 2 deficiency
  • ISD11 deficiency (Combined oxidative phosphorylation deficiency 19)
  • NFS1 deficiency (Infantile mitochondrial complex II/III deficiency – IMC23D)
  • Frataxin deficiency (Friedreich ataxia)

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