Skeletal muscle deformity is common in children with spastic cerebral palsy (CP), but the underlying mechanisms are unclear. This review explores some possible factors which may influence the development of muscle deformity in CP. Normal muscle function and growth appear to depend on the interaction of neuronal, endocrinal, nutritional, and mechanical factors, and also on the development of an appropriate balance between muscle protein synthesis and degradation, and between the development of contractile and non-contractile components. In this context, the changes seen in muscle in children with CP are reviewed and discussed. It is suggested that the development of muscle deformity in children with CP may be related to a multifactorial impairment of muscle growth, on which adaptation of the extracellular matrix due to altered loading may be imposed.Why do children with spastic cerebral palsy (CP) develop muscle deformity? We generally associate the development of deformity with the presence of spasticity and a consequent resistance of muscle to passive stretch, but the aetiology may be more complex. Children with CP show an early reduction in gastrocnemius muscle belly size, 1 an alteration in gene expression within the flexor carpi ulnaris, 2 an increase in sarcomere length, and an alteration in the extracellular matrix of semitendinosus.3 It is likely that the development of muscle deformity in spastic CP is related to a number of factors, but without detailed evidence are we able to speculate as to how it may occur? In this review, the factors influencing protein turnover in skeletal muscle are discussed, followed by an outline of the development of muscle innervation and of muscle fibre growth. Muscle changes in spastic CP are then discussed, following which some possible mechanisms which lead to the development of muscle deformity in CP are suggested.Neuronal innervation, mechanical demands, paracrine and endocrine factors, and nutrition influence skeletal muscle protein synthesis and degradation, which in turn determine muscle fibre size and metabolism. [4][5][6] The contractile proteins in the sarcomere, myosin and actin, are supported by larger proteins such as titin and nebulin, 7 which connect the actin and myosin, via the Z-disc and costameres, to the basal lamina and hence, via the endomysium, perimysium, and epimysium, to the tendon. Muscle fibres thus exist in a three-dimensional connective tissue framework which provides support, allows transmission of force, and appears to monitor muscle activity levels, particularly at the level of the Z-disc. 8,9 The balance between the development of muscle fibres and of the extracellular matrix in muscle appears to be determined by the interaction of neuronal, mechanical, and growth factors.