Meola G, Sansone V
Dipartimento di Neurologia, Università di Milano, Ospedale Clinicizzato San Donato, Italy.
Ital J Neurol Sci. 1996 Oct;17(5):347-53. doi: 10.1007/BF01999897.
The aim of this study is to describe the essential characteristics of a family affected by the newly-described proximal myotonic myopathy (PROMM) The clinical, laboratory and genetic findings are described and compared with those reported in the literature, and the clinical spectrum of the manifestations that are similar to but distinct from myotonic dystrophy (MD) is also explored. This has practical implications because the cases so far described suggest that the long-term prognosis with PROMM seems to be more favourable than that of patients with MD.
本研究的目的是描述一个受新发现的近端肌强直性肌病(PROMM)影响的家庭的基本特征。描述了临床、实验室和遗传学发现,并与文献报道的结果进行比较,还探讨了与强直性肌营养不良(MD)相似但又不同的临床表现谱。这具有实际意义,因为迄今为止所描述的病例表明,PROMM的长期预后似乎比MD患者更有利。