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OCR: e in which Adrenomyeloneuropathy is a rare disea dison's neurological deficit is associated with A nd disease. Patients may have both central cture may peripheral demyelination. The clinical with a be one of a spastic paraparesis associated ay be made peripheral neuropathy, and diagnosis n tured skin by analysis of long-chain fatty acids in cu trophy fibroblasts. In contrast to adrenoleucody which begins in childhood, ood. adrenomyeloneuropathy starts in adult ked These conditions are inherited as sex-lin ay precede recessive states, and Addison's disease r . When the neurological deficit in both disorder y produce adrenomyeloneuropathy develops, it m ion, subtle changes such as lack of concentra e disorder, behavioural disturbance, or a compulsi d. before more obvious focal signs are four