BIMDG

TEMPLE

 

 

 

Tools Enabling Metabolic Parents LEarning

Please note:
to view TEMPLE presentations as intended (with animation), please download and SAVE the PDF file to users own computer. Then open the downloaded file from your computer.

TEMPLE Guides

Argininosuccinic aciduria
Information for families following a new diagnosis

Citrullinaemia - what is it?
It is an inherited metabolic condition.

GA1 (glutaric aciduria type 1)
Information for families following a positive newborn screening

Galactosaemia
Information for families following a positive newborn screening

HCU (Homocystinuria)
Information for families following a positive newborn screening

HT1 (Hereditary Tyrosinaemia Type 1)
Information for families following a positive newborn screening

IVA (Isovaleric Acidaemia)
Information for families following a positive newborn screening

MCADD (medium chain acyl-CoA dehydrogenase deficiency)
Information for families following a positive newborn screening

MMA (Methyl Malonic Acidaemia)
Information for families following a positive newborn screening

MSUD (Maple Syrup Urine Disease)
Information for families following a positive newborn screening

OTC (Ornithine transcarbamylase deficiency)
Information for families following a new diagnosis

PKU (Phenylketonuria)
Information for families following a positive newborn screening

Propionic Acidaemia (PA)
Information for families following a positive newborn screening