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Inborn Errors of Metabolism program – application form B

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Publication date: 
2 September 2019
Last updated: 
4 March 2020
Publication type: 
Form
Intended audience: 
General public
Description: 

Individuals with the following conditions can use this form to apply for financial assistance under the Inborn Errors of Metabolism program:

  • HMG-CoA lyase deficiency
  • homocystinuria, not pyridoxine responsive (cystathionine β synthase deficiency)
  • lysinic protein intolerance (LPI)
  • maple syrup urine disease (MSUD)
  • ornithine amino transferase deficiency (hyperornithinaemia, gyrate atrophy of the retina)
  • hyperphenylalaninemia
  • tyrosinaemia: type I (hepatorenal tyrosinaemia, fumarylacetoacetate hydrolase deficiency), type II and type III
  • 3-methylcrotonyl-CoA carboxylase deficiency
  • cobalamin deficiencies (A, B, C and D)
  • glutaric aciduria type I (glutaryl CoA dehydrogenase deficiency)
  • isovaleric aciduria
  • methylmalonic acidaemia
  • propionic acidaemia
  • argininaemia (arginase deficiency)
  • argininosuccinicaciduria (ASA lyase deficiency)
  • carbamyl phosphate synthase (CPS)
  • citrullinaemia (ASA synthase deficiency)
  • N-acetylglutamate synthase (NAGS)
  • ornithine transcarbamylase deficiency (OTC).

Individuals diagnosed with dihydropteridine reductase (DHPR) deficiency, hyperphenylalaninemia or phenylketonuria (PKU) must use Form A. They must be reassessed and reapply for the program every 12 months.