This practical guide covers an introduction to complementary foods and transitioning to a concentrated low volume spoonable protein substitute, explore, in infants diagnosed with an amino acid disorder.
Collaboration with Anita MacDonald
Birmingham Children's Hospital, UK
Reviewed by Barbara Cochrane
Royal Hospital for Children, Glasgow, UK
Reviewed by Maureen Evans
Royal Children's Hospital, Melbourne, Australia
Want to access this resource?
OR LOGIN IF YOU ARE ALREADY REGISTERED
Rare disorders of protein metabolism
Glycogen Storage Disease
Paediatric Kidney Disease