Mahjneh I, Somer H, Paetau A, Marconi G
Department of Neurology, Pietarsaari Hospital, Pietarsaari, Finland.
Eur J Neurol. 2003 Jul;10(4):453-6. doi: 10.1046/j.1468-1331.2003.00616.x.
The authors carried out a clinical, laboratory and muscle computed tomographgy CT follow-up study of 18-21 years on two sisters affected by quadriceps myopathy (QM). The onset in the fourth decade was a weakness in the thighs. During the follow-up study, the patients showed only vasti muscles involvement, normal creatine kinase (CK) levels, myopathic muscle biopsy and electromyography (EMG) and normal membrane protein expression on immunocytochemical analysis. Therefore, all muscle pathologies known to have quadriceps involvement as a leading feature have been ruled out. We conclude that our patients have pure QM with probable autosomal recessive inheritance.
