Linkage Between Chronic Granulomatous Disease and Duchenne's Muscular Dystrophy?

Sir .—I read with interest the letter by Schmidt et al (Journal1981;135:376-377), because I recently studied a case of chronic granulomatous disease that had a diagnostic difficulty of a somewhat different nature. Report of a Case .—A 2-year-old boy was diagnosed as having chronic granulomatous disease based on the clinical pattern of recurrent staphylococcal infections since birth, including impetigo three times and a left anterior cervical abscess. He also had had pneumonia, but no organism was isolated on lung needle biopsy. The quantitative nitro blue tetrazolium test (NBT) showed a resting value of 0.027 and phagocytic value of 0.039 (normal, resting, 0.100 ± 0.075; phagocytic 0.300 ± 0.050). The bactericidal assay showed a marked inhibition in the intracellular killing of Staphylococcus aureus 502-A. Long-term prophylaxis with sulfamethoxazole-trimethoprim (Bactrim) has kept the patient free of infection. At 3 years of age, a positive Gowers' sign and pseudohypertrophy of the calves