background: the pelger-huet anomaly dominantly is a rare and benign inherited defect of terminal neutrophil differentiation. although neutrophil migration may be minimally impaired, granulocytes function is otherwise normal association abnormalities such as ocular, musculoskeletal are reported very rare. case: an eight year-old boy with good consciousness but severe muscular atrophia and diffic...

Background: The Pelger-Huet anomaly dominantly is a rare and benign inherited defect of terminal neutrophil differentiation. Although neutrophil migration may be minimally impaired, granulocytes function is otherwise normal association abnormalities such as ocular, musculoskeletal are reported very rare. Case: An eight year-old boy with good consciousness but severe muscular atrophia and diffic...

Background: LAMA2-muscular dystrophy (LAMA2-MD) is an autosomal recessive disease, and the most common form of congenital muscular (CMD). Most patients develop a disease characterized by inability to achieve walking capacity, multiple joint deformities, respiratory insufficiency, some degree dysphagia. However, there gravity spectrum, never sitting position, while others can walk unassisted. Th...

background: it is widely recognized that neuromuscular function is temperature sensitive. changes in muscle temperature may affect muscle force development. the aim of this study was to investigate the effects of temperature on wrist flexor muscles endurance. methods: fifteen healthy subjects (mean age  21.13 ±1.30 years) participated in the present study.  the wrist flexor muscles endurance wa...