CARPAL TUNNEL SYNDROME IN THE MUCOPOLYSACCHARIDOSES AND MUCOLIPIDOSESF. S. Haddad, BSc, FRCS, Senior Orthopaedic Registrar; D. H. A. Jones, FRCS Orth, Consultant Orthopaedic Surgeon; A. Vellodi, FRCP, Consultant Physician; N. Kane, MD, FRCS, Senior Registrar in Neurophysiology; and M. C. Pitt, MD, FRCP, Consultant NeurophysiologistThe Hospital for Sick Children, Great Ormond Street, London WC1N 3JH, UK. Correspondence should be sent to Mr F. S. Haddad at 46B Hanover Gate Mansions, Park Road, London NW1 4SN, UK. Children with a mucopolysaccharidosis or mucolipidosis suffer progressive disability of the hands, particularly in relation to dysfunction of the median nerve. This is an increasing problem because bone-marrow transplantation has dramatically improved survival without apparently changing the musculoskeletal manifestations. We have reviewed 48 children with these syndromes who required carpal tunnel decompression, recording symptoms, signs, radiological, electrophysiological and operative findings, histology and upper-limb function. In these children the carpal tunnel syndrome differs from that seen in adults. Symptoms are rare but signs such as decreased sweating, pulp atrophy, thenar wasting and manual clumsiness are much more common. At operation, the flexor retinaculum was thickened and a mass of white tenosynovium engulfed the flexor tendons. Most patients had some definite nerve constriction with a thickened epineurium. Functional improvement was seen after early decompression, with some benefit from simultaneous tendon release. Regular physiotherapy helped to maintain increased hand movement. We describe our assessment protocol, the physiotherapy and operative regime and the standard functional review which helps to maximise function in the hands and upper limbs of these children.
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