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CaF directory of specific conditions and rare syndromes
Condition usually commencing between 3 and 8 months of age characterised by infantile spasms and often associated with a change in behaviour and a slowing of development of the child.
CaF directory of specific conditions and rare syndromes
A genetic condition causing developmental delay. Features include facial similarities (prominent cheeks, upturned nose, wide mouth, irregular teeth) and hypersensitivity to loud noises. Children may have a heart problem and some develop hypercalcaemia (low calcium levels) within the first 2 years of life.