DISCLAIMER – Terms and Conditions of Use
There is very little evidence base for the management of inborn errors so this information has been written taking into account what is regarded as the current best practice. It has been scrutinised carefully but there may still be errors. Furthermore new evidence at any time can invalidate this information. No liability whatsoever can be taken as a result of using this information.
Nursing Guidelines
- Guideline foreword
- Nursing Guidelines – management of children with Glutaric Aciduria Type 1
- Nursing Guidelines – management of children with Fatty Acid Oxidation Defect
- Nursing Guidelines – management of children with Glycogen Storage Disease Type 3
- Nursing Guidelines – management of children with MSUD
- Nursing Guidelines – management of children with Methylmalonic Aciduria
- Phenylketonuria PKU
- Nursing Guidelines – management of children with HCU
- Nursing Guidelines – management of children with Galactosaemia
- Nursing Guidelines – management of children with Propionic Aciduria
- Nursing Guidelines – management of children with Urea Cycle Disorders
- Nursing Guidelines – management of children with Classical Phenylketonuria 2018
Nursing Care Plans
- Phenylketonuria New Diagnosis
- Galactosaemia
- Homocystinuria (HCU) New Diagnosis Care Plan
- Hyperammonaemia Care Plan
- Potential Actual Altered Neuro function secondary to Hyperammonaemia
- Maple Syrup Urine Disease Guidelines 2022
- Maple Syrup Urine Disease Elevated BCAAs
- Glycogen Storage Disease Type III
- Altered Nutritional Requirements Glutaric Aciduria Type 1
- Altered Nutritional Requirements – Methylmalonic aciduria (MMA) & Propionic aciduria (PA) Care Plan
- Urea Cycle Defect New diagnosis
- Glutaric Aciduria Type 1 (GA1) (New Diagnosis)
- Metabolic Investigations
Metabolic Calculations Booklet