فایل ورد کامل پاتوفیزیولوژی انقباض های عضلانی در فلج مغزی

توجه : به همراه فایل word این محصول فایل پاورپوینت (PowerPoint) و اسلاید های آن به صورت هدیه ارائه خواهد شد

این مقاله، ترجمه شده یک مقاله مرجع و معتبر انگلیسی می باشد که به صورت بسیار عالی توسط متخصصین این رشته ترجمه شده است و به صورت فایل ورد (microsoft word) ارائه می گردد

متن داخلی مقاله بسیار عالی، پر محتوا و قابل درک می باشد و شما از استفاده ی آن بسیار لذت خواهید برد. ما عالی بودن این مقاله را تضمین می کنیم

فایل ورد این مقاله بسیار خوب تایپ شده و قابل کپی و ویرایش می باشد و تنظیمات آن نیز به صورت عالی انجام شده است؛ به همراه فایل ورد این مقاله یک فایل پاور پوینت نیز به شما ارئه خواهد شد که دارای یک قالب بسیار زیبا و تنظیمات نمایشی متعدد می باشد

توجه : در صورت مشاهده بهم ریختگی احتمالی در متون زیر ،دلیل ان کپی کردن این مطالب از داخل فایل می باشد و در فایل اصلی فایل ورد کامل پاتوفیزیولوژی انقباض های عضلانی در فلج مغزی،به هیچ وجه بهم ریختگی وجود ندارد

تعداد صفحات این فایل: ۱۲ صفحه

بخشی از مقاله انگلیسیعنوان انگلیسی:Pathophysiology of Muscle Contractures in Cerebral Palsy~~en~~

INTRODUCTION

Nature of the Problem

Cerebral palsy (CP) is a motor disorder caused by a nonprogressive injury to the developing brain.1 The injury occurs perinatally and, though causes are rarely known,2,3 CP is common in infants born preterm with small birth weights.4 CP occurs in 2 to 3 of every 1000 live births5 and has heterogeneous symptoms, anatomic involvement, and functional impairment, including lifelong changes in motor function.1,2 These alterations stem from both changes in the neural drive to muscles6 and changes to muscles themselves.

Symptoms

Spastic CP, which involves injury to the pyramidal system, is the most common form of CP, making up nearly 75% of all cases.3 Spasticity has been defined as a “velocity dependent resistance to stretch.”۷ Limb involvement varies, with patients showing symptoms in either all 4 limbs (tetraplegia or quadriplegia), primarily on one side of the body including one upper and lower extremity (hemiplegia), or primarily in the lower extremities (diplegia).8 Patients’ functional mobility can be classified using several rating scales, including the Gross Motor Function Classification System (GMFCS), which rates patient mobility on a scale of 1 to 5 from high to low function, respectively.1,3 Although the injury associated with CP initially occurs in the developing brain, symptoms are commonly treated at the muscle level. Because the population affected with CP is large and heterogeneous, a better understanding, especially among clinicians and therapists, of muscular adaptations in CP may lead to improvements in treatment or even development of completely novel therapeutic strategies. To understand the adaptations that occur in muscle from CP patients, it is important to review the function of typically developing muscle.

HEALTHY SKELETAL MUSCLE STRUCTURE AND FUNCTION

Muscle Structure

The fundamental unit of muscle force production is the sarcomere. Sarcomeres produce force by the interaction between 2 proteins, actin and myosin. Force production is affected by both muscle velocity and the amount of overlap between these 2 proteins, or sarcomere length. The sarcomere length-tension relationship has been characterized in the lengthtension curve.9 Sarcomeres are joined end to end (in series) to form myofibrils. Bundles of myofibrils form myofibers, or multinucleated muscle cells. These muscle fibers are joined into muscle fiber bundles, or fascicles (Fig. 1). At each increasing size scale, extracellular matrix (ECM), the surrounding connective tissue, encapsulates muscle structures. Endomysium surrounds individual myofibers,10 perimysium surrounds muscle fascicles,11 and epimysium surrounds the whole muscle (see Fig. 1).12,13 The composition and arrangement of these structures is important to muscle function, and can vary in muscle disorders. The extensive growth and regeneration capacity seen in muscle is due to its intrinsic stem cell population. Most of these stem cells are called satellite cells14 and are found below the basal lamina of myofibers; they are normally quiescent except when activated during times of muscle disease or injury.15 Satellite cell number and viability, rather than being constant throughout life, decreases with age or diseases that are characterized by extensive regeneration.16 Conditions such as muscular dystrophy, which require constant regeneration of muscle fibers, are believed to eventually lead to exhaustion of the satellite cell population17 and the concomitant loss in a muscle’s ability to adapt to the new functional demand.

$$en!!