Essays on Subacute

Post-stroke dysphagia, a potentially fatal complication, affects an estimated 23-50% of all stroke survivors. It is associated with a seven fold increase in the risk for aspiration pneumonia. Aspiration pneumonia increases the catabolic demands of the body and in the settings of impaired swallowing leads to a vicious cycle of malnutrition, dehydration, and further infections (Shaker & Geenen, 2011). Dysphagia affects a significant number of patients with hemispheric stroke which is the main subtype of ischemic stroke in the general population (Kumar et al., 2011). The functions of swallowing are subserved by a vast brain network. The inferior peri-rolandic sensorimotor ...

Introduction

Doctors, nurses, and other medical personnel have a series of duties that they must attend to, and one of them is dealing with patients’ medical grievances. Many of these complaints are quite common, ranging from the mundane to life-threatening. However, it is the job of these medical personnel to pay attention to these complaints, as these are the symptoms and underlying causes of the true medical condition of the patient. Knowing what these complaints mean will prove to be useful in a patient’s diagnosis. In some cases, this can mean the difference between life and death because some ...

INTRODUCTION

In the modern era there are a plethora of diseases, conditions and disorders that can affect individual’s health, well-being and quality of life for people all across the world. Whether it is from cancer to infections or from diabetes to HIV there is always the possibility of contracting or developing disease. However, not all diseases are contracted or developed due to an external influence, there are some that originate from the inside; such conditions are generally referred to as an autoimmune disease. This means that the problem involves an individual’s own immune system, perceives their own body ...

Abstract

Tay-Sachs disease (TSD) is a group of autosomal recessive lipid lysosomal storage disorders caused by mutations of the HEXA gene, which codes for the alpha subunit of the enzyme Hexosaminidase A, one of three enzymes responsible for the normal degradation of GM2 ganglioside, a substance found in high concentration in the plasma membrane of neuronal cells. The classic acute infantile form, discussed here, is a neurodegenerative disorder with onset at four to eight months of age in which acquired capabilities are lost and general neurologic deterioration occurs, with death by age two to four years. It occurs with highest frequency in the ...