EhlersDanlos Syndrome :: essays papers

EhlersDanlos SyndromeEhlers-Danlos sydrome (explosive detection system) is a r be catching group of co-occurrence tissue disorders characterized by defects of the major structural protein in the body (collagen). Collagen is a tough ropy protein that plays an essential role in binding, holding together, streng and thening, and providing snap to bodily cells and tissues. in that location be six major types of explosive detection system that I will discuss, as yet I will only go into exposit discussion on deuce of the six types of explosive detection system. The two major types of explosive detection system are determinate EDS and Hyper smooth EDS. These two types make up 90% of all EDS cases. I will discuss the general symptoms of these two types along with pathology, then diagnostic factors, and the different treatments for this disorder (Smith).EDS privy vary in severity and are transmitted as autosomal recessive, autosomal dominant, or X-linked recessive traits. The prima ry characteristics are hyperextensible carm and joints (Dia. 1-2, pg.6), disposition to bruise slow (Dia. 3, pg.6), reduced wound healing capability, pseudotumors, and ocular defects. Differences deep down the six types whitethorn reflect inter/intra familial variability or genetic heterogeneity. for each one type of EDS is classified symptoms and signs that are resulted (Clarke, D., Skrocki-Czerpak, K., Neumann-Potash, L).thither are some six types of EDS that have been distinguished simply other types come through that are very unparkland. Classical, Hypermobile, Vascular, Kyphoscoliosis, Arthrochalasia, and Dermatosparaxis. Classical and Hypermobile make up over 90% of all reported cases of EDS. With the Classical type of EDS a somebody would have hyperextensible (stretchy) skin with widened atrophic scars and joint hypermobility. The skin is smooth and smooth with tissue fragility and easy brusability. Also manifest are molluscoid pseudotumors (fleshy lesions associat ed with scars) a great deal found over pressure points (e.g. elbows) and subcutaneous spheroids, which are commonly mobile and palpable on the forearms and shins. Complications of joint hypemobility include sprains, hurly burly are common in the shoulder, patella and temporomandibular joints Muscle hypotonia and sluggish gross aim development also can occur It is inherited in an autosomal dominant manner (Clarke, D., Skrocki-Czerpak, K., Neumann-Potash, L.).In the Hypermobile type of EDS the joints of the body aim Hypermobility, which is the dominant clinical manifestation. General joint hypermobility affects king-size (elbows, knees) and small (fingers and toes) joints are evident. Skin is hyperextensible, smooth/velvety, and bruising occurs easily as well. Reoccurring joint dislocations are common, and joints such as shoulder, patella, and temporomandibular joint dislocate frequently. chronic joint and limb pain is a common amongst individuals with Hypermobile type EDS.Ehle rsDanlos Syndrome essays coverEhlersDanlos SyndromeEhlers-Danlos sydrome (EDS) is a rare inherited group of connective tissue disorders characterized by defects of the major structural protein in the body (collagen). Collagen is a tough fibrous protein that plays an essential role in binding, holding together, strengthening, and providing elasticity to bodily cells and tissues. There are six major types of EDS that I will discuss, however I will only go into detailed discussion on two of the six types of EDS. The two major types of EDS are Classical EDS and Hypermobile EDS. These two types make up 90% of all EDS cases. I will discuss the general symptoms of these two types along with pathology, then diagnostic factors, and the different treatments for this disorder (Smith).EDS can vary in severity and are transmitted as autosomal recessive, autosomal dominant, or X-linked recessive traits. The primary characteristics are hyperextensible skin and joints (Dia. 1-2, pg.6), tendency to bruise easily (Dia. 3, pg.6), reduced wound healing capability, pseudotumors, and ocular defects. Differences within the six types may reflect inter/intra familial variability or genetic heterogeneity. Each type of EDS is classified symptoms and signs that are resulted (Clarke, D., Skrocki-Czerpak, K., Neumann-Potash, L).There are approximately six types of EDS that have been distinguished but other types exist that are very uncommon. Classical, Hypermobile, Vascular, Kyphoscoliosis, Arthrochalasia, and Dermatosparaxis. Classical and Hypermobile make up over 90% of all reported cases of EDS. With the Classical type of EDS a person would have hyperextensible (stretchy) skin with widened atrophic scars and joint hypermobility. The skin is smooth and velvety with tissue fragility and easy brusability. Also evident are molluscoid pseudotumors (fleshy lesions associated with scars) frequently found over pressure points (e.g. elbows) and subcutaneous spheroids, which are commonly mob ile and palpable on the forearms and shins. Complications of joint hypemobility include sprains, dislocation are common in the shoulder, patella and temporomandibular joints Muscle hypotonia and slower gross motor development also can occur It is inherited in an autosomal dominant manner (Clarke, D., Skrocki-Czerpak, K., Neumann-Potash, L.).In the Hypermobile type of EDS the joints of the body experience Hypermobility, which is the dominant clinical manifestation. General joint hypermobility affects large (elbows, knees) and small (fingers and toes) joints are evident. Skin is hyperextensible, smooth/velvety, and bruising occurs easily as well. Reoccurring joint dislocations are common, and joints such as shoulder, patella, and temporomandibular joint dislocate frequently. Chronic joint and limb pain is a common amongst individuals with Hypermobile type EDS.