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Complete Information on Esotropia Esotropia is a type of strabismus. Esotropia is a type of deviation of alignment of strabismus or eye. Esotropia is a centripetal rotation two eyes. In the esotropia, one or the two eyes turns inside towards the nose. Complete Information on Esophageal Varices Esophageal varices are the blood vessels dilated in the wall of the esophagus. Esophageal varices develop when the normal flow of blood to the liver is blocked. Blood supports then in smaller, more fragile blood vessels in the oesophagus, and sometimes in the stomach or the rectum, making inflate the ships. Complete Information on Esophageal Atresia Esophageal atresia is a condition in which a part of the oesophagus misses. Esophageal atresia is often associated another congenital anomalies, anomalies most generally cardiac. Complete Information on Erythropoietic Protoporphyria Erythropoietic protoporphyria (EPP) is a rare disorder dominating autosomal. Protoporphyria d' Erythropoietic (EPPalso called is the disease and the porphyrias gunther . Complete Information on Erythromelalgia Erythromelalgia is a disease rare and characterized by the redness of the skin, the enlarge temperature, and the pain in the ends (of the feet and the hands), which usually occurs in response to heat and the moderate exercise. Complete Information on Erythema Multiforme Erythema multiforme is a disorder of skin follow of an allergic reaction. Erythema multiforme is attenuated by the deposit of immunized complex in the microvascularisation outside of the skin and the oral mucous membrane which follows usually an infection or a preceding exposure of drug. Complete Information on Erysipelas Erysipelas is also known as fire of saint anthony. Erysipelas is a surface infection of the skin. Erysipelas is having for result the ignition and to advance caractéristiquement with large fundamental fabric. Complete Information on Epstein Barr Virus Epstein-Barr Virus (EBV), also called Human herpesvirus 4 (HHV-4). The virus of Epstein-Barr (EBV) is a human virus common that mononucleosis and infectious plays of causes a role in the appearance of the two rare shapes of cancer: Lymphoma of Burkitt , and nasopharyngeal carcinome. Complete Information on Epilepsy Epilepsy is a physical state which starts in the brain. Epilepsy is characterized by recurring unprovoked seizures. Sometimes seizures are related to a provisional state, such as the exposure to drugs, the withdrawal of certain drugs, or the abnormal levels of sodium or glucose in blood. Complete Information on Epidermolysis Bullosa Epidermolysis Bullosa is a condition of formation of blisters which changes considerably under severity and the forms. The simplex of bullosa of Epidermolysis (EBS) comprises separation intraepidermal skin. Complete Information on Epidermodysplasia Verruciformis Epidermodysplasia verruciformis(EV) is a rare disease héritable. This disease is characterized by the chronic infection with the human papillomavirus (HPV). Complete Information on Ependymoma Ependymomas are a rare type of glioma. They can be found in any part of the brain or of the spine but most generally are found in the principal part of the brain. Complete Information on Eosinophilic Fasciitis Eosinophilic fasciitis is characterized by tenderness and swelling of the ends caused by the ignition of the fasce and the muscles. The arms, the legs, the trunk, and the face can be affected by diminish, weakness of muscle, and the common changes of the overlying skin. Complete Information on Enterobiasis Enterobiasis also known infection of pinworm. Enterobiasis is an intestinal infection caused by the ascaride lombricoïde parasite called the vermicularis of Enterobius. Enterobiasis is the infection of worm most common to the United States. Complete Information on Endometrial Cancer Endometrial cancer can sometimes indicated of uterine cancer. Endometrial cancer is the cancer which starts in endometrium, the lining of the uterus (uterus). Uterine cancer, the malignant neoplasm most common of the female genital area and the quarter majority of common cancer among women. Complete Information on Endocarditis Endocarditis is a rare state which causes the ignition of the lining of heart, the muscles of heart and the valves of heart. Endocarditis can be classified by the etiology like infective or not-infective. Complete Information on Encephalocele Encephalocele known cranium bifidum. It is a defect neural of tube and characterized by bag-like projections of the brain and the membranes which cover it by openings in cranium. Complete Information on Encephalitis Lethargica Encephalitis lethargica is a definite infectious disease of the nervous system. The cause of encephalitis lethargica is not known for some. Several of the people with encephalitis lethargica had tested recent pharyngitis. Complete Information on Empty Sella Syndrome Empty sella syndrome is a condition in which the pituitary gland narrows or becomes flattened. Empty sella syndrome is common among women who are excessive weight or have hypertension. Complete Information on Emphysema Emphysema is a type of obstructive pulmonary disease chronic (COPD). The emphysema is a lung disease which implies damage with the bags of air (cells) in the lungs. Complete Information on Elastosis Perforans Serpiginosa Elastosis perforans serpiginosa is also called Lutz-Miescher's syndrome. Elastosis perforans serpiginosa is a disorder characterized by transepithelial elimination of elastin. Complete Information on Eisenmenger Syndrome Eisenmenger syndrome develops in the individuals with expressive defects of heart. People who have Eisenmenger are usually constant with a large hole in the heart. Complete Information on Ehrlichiosis Ehrlichiosis is a disease acute and caused by ehrlichia of bacteria. Ehrlichiosis is most common to spring and the summer. The signs and the symptoms of the ehrlichiosis extend from the soft evils of body to the fever engraves and usually appear in a week or two of a bite of drill. Complete Information on Ehlers-Danlos Syndrome The syndrome of Ehlers-Danlos (EDS) is the name given to a group of disorders héritables of connective fabric. This disorders characterized by defects of principal structural protein in the body (collagenous). Complete Information on Edwards Syndrome Edwards ' also known syndrome under the name of 18 trisomy. Edwards ' genetic chromosomal disorder rare of syndrome occurs when a child is constant with three copies of chromosome 18, rather than the two usual ones. Complete Information on Ectopic Pregnancy A ectopic pregnancy is an abnormal pregnancy which occurs apart from the uterus (uterus). The ectopic pregnancy is a complication of pregnancy in which the fertilized ovule is established in any fabric other than the uterine wall. Complete Information on Ectrodactyly Ectrodactyly, generally known under the name of lobster claw syndrome. Ectrodactyly is often combined with the dysplasy of Ectodermal and split Lip/Palate like syndrome of the EEC. Complete Information on Ectodermal Dysplasia The dysplasia of Ectodermal it is one be hereditary characterized through abnormal development of the skin, hats, the nail, the teeth and the glands of the sweat. Complete Information on Eclampsia Eclampsia is a difficult situation of pregnancy and is characterised by convulsions. Eclampsia is not the cause of seizures that occur during the first trimester (term of three months) or well into the postpartum period. Complete Information on Ebstein's Anomaly Ebstein's anomaly, also known ebstein's malformation. Ebstein's Anomaly is an extremely rare heart defect of the tricuspid valve. It firstly includes the lower right chamber of your heart and the tricuspid valve the valve between the upper right chamber (atrium) and the right ventricle. Complete Information on Eales Disease Eales disease is well known an idiopathic obliterative vasculopathy. Eales disease is common found in India. Eales Disease is a rare disorder of sight that seem as an inflammation and white haze around the outercoat of the veins in the retina. Complete Information on Eagle's Syndrome Eagle syndrome is medically name as the elongation of the styloid method and stylohyoid ligament calcification. Eagle syndrome is an accumulate of symptoms caused by an elongated ossified styloid process. Complete Information on Afibrinogenemia with Treatment and Prevention Afibrinogenemia is a occasional congenital blood disorder in which the blood does not coagulation normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation. Complete Information on Advanced sleep phase syndrome with Treatment and Prevention Advanced sleep phase syndrome (ASPS) is a condition in which patients feel very sleepy early in the evening and wake up very early in the night. The disorder is more likely to appear in the elderly. Complete Information on Acute promyelocytic leukemia with Treatment and Prevention Acute promyelocytic leukemia, a malignancy of the ivory marrow in which there is an inadequacy of old blood cells in the myeloid cable of cells and a surplus of immature cells called promyelocytes. Complete Information on Acute myelocytic leukemia with Treatment and Prevention Acute myeloid leukemia (AML), is a cancer of the myeloid line of white blood cells. It is transparent by the rapid proliferation of abnormal cells which accumulate in the bone marrow and interfere with the production of normal blood cells. Complete Information on Acute mountain sickness with Treatment and Prevention Acute mountain sickness is an sickness that can affect mountain climbers, hikers, skiers, or travelers who climb too fast. Acute mountain sickness is actually more common in fit young men because they are more likely to attempt a rapid ascent by racing up the mountain like some indestructible super hero. Complete Information on Acute intermittent porphyria with Treatment and Prevention Acute sporadic porphyria(AIP) is an uncommon metabolic disorder in the output of heme, the oxygen-binding prosthetic group of hemoglobin. Acute sporadic porphyria is an autosomal predominant disease that results from defects in the enzyme porphobilinogen-deaminase. Complete Information on Acrodysostosis with Treatment and Prevention Acrodysostosis is an extremely rare congenital malformation syndrome which involves shortening of the knuckles of the legs and hands, in approximately 90% of affected children, and peculiar fecies. Complete Information on Acrodermatitis enteropathica with Treatment and Prevention Acrodermatitis enteropathica is a rare genetic disorder, especially in pediatric and dermatology clinics. It is caused by an inability to absorb sufficient zinc from the diet. Zinc deficiency may be due to inadequate intake, malabsorption, excessive loss, or a combination of these factors. Complete Information on Acral lentiginous melanoma with Treatment and Prevention Acral lentiginous melanoma also known as also known as subungual melanoma, is a kind of skin melanoma. Acral lentiginous melanoma is seen on the palms, soles and under the nails. Complete Information on Acquired ichthyosis with Treatment and Prevention Acquired ichthyosis is a disorder clinically and histologically similar to ichthyosis vulgaris. Acquired ichthyosis most often appears in adulthood. It may appear before or after the diagnosis of a systemic condition. Complete Information on Acquired angioedema with Treatment and Prevention Acquired angioedema is a hypersensitivity disorder that presents as edema of the subcutaneous tissues and mucosa, typically involving the upper airways or gastrointestinal tract, and often accompanied by urticaria. Complete Information on Acquired agranulocytosis with Treatment and Prevention Acquired agranulocytosis is a circumstance that results from bankruptcy of a person's ivory marrow to develop an adequate amount of light-colored blood cells, or increased devastation of the light-colored blood cells. Complete Information on Acanthamoeba infection with Treatment and Prevention Acanthamoeba are microscopic ameba commonly found in the environment. Acanthamoeba are ubiquitous organisms and have been isolated from soil, water, air, and dust. Complete Information on Acalvaria with Treatment and Prevention Acalvaria is an uncommon inborn deformity in which the thin bones of the cranial hurdle, duramater and associated muscles are missing but the key anxious structure is normally untouched. Complete Information on Ablepharon macrostomia syndrome with Treatment and Prevention Ablepharon macrostomia syndrome is an exceedingly uncommon inherited hereditary disorder. The precise reason of Ablepharon macrostomia syndrome is not amply understood, some cases indicate that the disorder may be inherited as an autosomal recessive hereditary trait. Complete Information on Abetalipoproteinemia with Treatment and Prevention Abetalipoproteinemia (ABL) is an extremely rare autosomal recessive disorder, caused by mutations of the microsomal triglyceride-transfer protein gene. Abetalipoproteinemia interferes with the normal absorption of fat and fat-soluble vitamins from food. Complete Information on Aase Smith syndrome with Treatment and Prevention Aase syndrome or Aase-Smith syndrome is a rare inherited disorder. A familial deformity syndrome of variable expressivity, characterised by congenital hypoplastic anaemia and connatal triphalangy of the thumbs. Complete Information on Aarskog syndrome with Treatment and Prevention Aarskog syndrome is an inherited disease. The Aarskog-Scott syndrome is a disorder with brief height, hypertelorism, downslanting palpebral fissures, anteverted nostrils, multilateral laxity, shawl scrotum, and psychological retardation. Complete Information on Aagenaes syndrome with Treatment and Prevention Aagenaes syndrome is due to congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant-cell hepatitis with fibrosis of the portal tracts. Complete Information on Creutzfeldt Jakob disease Creutzfeldt-Jakob disease (CJD) is aform of brain damage that causes a rapid decrease of mental function and movement. It isbelieved to result froma protein called a prion. It affects about one person in every one million people per year worldwide. Complete Information on CREST syndrome CREST (Limited scleroderma) is a kind of Systemic Sclerosis (scleroderma) which is characterized by Calcinosis , normally in the fingers. Scleroderma is a chronic disease characterized by undue deposits of collagen in the rind or new organs. Complete Information on Cretinism Cretinism is a circumstance of seriously stunted physiological and psychological increase payable to raw inborn inadequacy of thyroid hormones. Cretins have dwarfed bodies, with curvature of the backbone and pendulous stomach. Complete Information on Craniosynostosis Craniosynostosis is a birth defect of the brain. Craniosynostosis consists of premature fusion of 1 or more cranial sutures, often resulting in an abnormal head shape. Complete Information on Colitis Colitis too called ulcerative colitis. It is an intense or chronic inflammation of the membrane lining the colon your big bowel or intestine. Common symptoms associated with colitis are abdominal cramping, regular lax stools or relentless diarrhoea, departure of command of intestine role, fever, sleepiness, and weight departure. Complete Information on Cutis laxa Cutis laxa too called elastolysis. It is a group of uncommon connective tissue disorders in which the rind becomes inelastic and hangs broadly in folds. Cutis laxa can be balmy, affecting simply an individual's show, or serious, affecting the domestic organs. Complete Information on Copper deficiency Copper is essential in the proper development of the central nervous system, correct bone growth, and hair pigmentation. Copper-deficient goats have difficulty conceiving kids and, if bred, abortions are not uncommon. Complete Information on Coxa vara, congenital Coxa vara usually presents with a limp, and limited ability to bring the thigh out to the side. Coxa vara includes all forms of decrease of the femoral neck shaft angle to less than 120-135°. Congenital coxa vara (CCV), also referred tocervical coxa vara. Complete Information on Choroid plexus cysts Choroid plexus cysts (CPCs) are cysts that occur within choroid plexus of the brain. Choroid plexus cysts (CPC's) are sometimes found on ultrasound scan at around 18 to 20 weeks gestation. Complete Information on Choroid plexus papillomas Choroid plexus papillomas are one of the most common tumors of the nervous system in infants. The most frequent early symptoms, megalocephalia and vomiting, caused by elevated intracranial pressure often lead to a diagnosis only at a critical clinical stage. Complete Information on Chondroblastoma (benign) Chondroblastomas are rare epiphyseal bone tumors. It is found in the epiphysis of long bones, usually of the lower extremity. The tumor has a preference for males over females and the mean age of presentation is approximately 20 years old. Complete Information on Chronic granulomatous disease Chronic granulomatous disease is inherited disorder of phagocytic cells. These cells usually destroy bacterium. Chronic granulomatous disease causes repeated bacterial. Complete Information on Ceroid lipofuscinosis neuronal The neuronal ceroid lipofuscinoses (NCLs), also known as batten disease. Neuronal ceroid lipofuscinoses (NCLS) refers to a group of uncommon, inherited disorders of the brain cells. Complete Information on Chaotic atrial tachycardia Multifocal atrial tachycardia, also designated "chaotic atrial tachycardia,". Multifocal atrial tachycardia (MAT) is an arrhythmia with an irregular atrial rate greater than 100 beats per minute (bpm). Complete Information on Chandler's syndrome Chandler's syndrome (CS) is a rare eye disorder. Chandler's syndrome (CS) is caused herpes. The problem is that the corneal endothelium (which lines the inside of the cornea) grows outward and over the trabecular meshwork. Complete Information on Chondrosarcoma Chondrosarcoma is a bone cancer types. Chondrosarcoma is a cartilage-based tumor and is in a category of cancers called sarcomas. Chondrosarcomas occur primarily in adults, is rarely encountered during the adolescent years and almost never affects young children. Complete Information on Chikungunya Chikungunya is a relatively rare form of viral fever caused by an alphavirus that is spread by mosquito bites. The disease resembles dengue fever, and is characterized by severe, sometimes persistent, joint pain(arthitis) , as well as fever and rash. Complete Information on Chicken pox Chickenpox is a common illness among kids, particularly those under age 12. Chickenpox is caused by a virus called the varicella-zoster virus (varicella is the medical name for chickenpox). Complete Information on Cherubism Cherubism is genetic disorder of childhood. It is characterized by abnormal bone tissue in the lower part of the face. Cherubism is due to a problem in bone composition that is largely limited to the upper and lower jaws with loss of bone in the jaws and its replacement by excessive amounts of fibrous tissue Complete Information on Chancroid Chancroid is a common sexually transmitted disease (STD) caused by infection with the Gram negative bacterium Haemophilus ducreyi, a fastidious organism primarily located in the extra cellular spaces. Complete Information on Cholestasis Cholestasis simply means failure of flow of bile. Bile formation is a secretory function of the liver. It begins in bile canaliculi that form between two adjacent surfaces of liver cells (hepatocytes) similar to the terminal branches of a tree. Complete Information on Cholera Cholera is also known as epidemic cholera. Cholera is a bacterial disease that affects the intestinal parcel. It is caused by a microbe called Vibrio cholerae. Complete Information on Choledochal cyst A choledochal cyst is an uncommon inborn dilation of the hepatic or bile duct of the liver, the parcel which transports bile produced by the cells to the gallbladder and duodenum. Complete Information on Cholecystitis Cholecystitis is inflammation of the gallbladder. Cholecystitis is usually caused by a gallstone in the cystic duct, the duct that connects the gallbladder to the hepatic duct. Complete Information on Chalazion A chalazion (stye) is a small lump in the eyelid caused by obstruction of an oil producing or meibomian gland. Chalazia may occur in the upper or lower lids, causing redness, swelling and soreness in some cases. Complete Information on Central pontine myelinolysis Central pontine myelinolysis is heart harm caused by the devastation of the bed (myelin sheath) covering heart cells in the brainstem. Common reason is the speedy correction of reduced blood sodium levels (hyponatremia). Complete Information on Celiac disease The Celiac disease is the active immunity confusion. The Celiac disease is also calls celiac sprue, nontropical sprue, with gluten sensitive enteropathy. Complete Information on Catastrophic Antiphospholipid Syndrome Catastrophic antiphospholipid syndrome (CAPS) is an uncommon kind of antiphospholipid syndrome resulting in multiorgan bankruptcy with a mortality pace of about 50. Complete Information on Epidermodysplasia verruciformis with Treatment and Prevention Epidermodysplasia verruciformis (EV) is an uncommon inherited disease. The disease seems to be caused by several distinct man papillomaviruses. It is a lifelong, viral-mediated, autosomal recessive disorder affecting the skin. Complete Information on Ependymoma with Treatment and Prevention Ependymomas are tumors that originate from the ependyma. Ependymomas are an uncommon character of glioma. They produce from the ependymal cells which line the ventricles and from the key canal of the spinal cord. Complete Information on Enterobiasis with Treatment and Prevention Enterobiasis or pinworm infection is a common, contagious, parasitic infestation found mainly in children. The disorder is spread by swallowing or inhaling the tiny eggs of the pinworm. It occurs especially in children. Complete Information on Endometrial cancer with Treatment and Prevention Endometrial cancer is one of the almost popular cancers in American women. In endometrial cancer, cancer cells produce in the lining of the womb. Why these cancer cells produce is not completely known. Complete Information on Endocarditis with Treatment and Prevention Endocarditis is an inflammation of the inner bed of the eye, the endocardium. Endocarditis may be classified by etiology as either infective or non-infective, depending on whether a microorganism is the origin of the trouble. Complete Information on Encephalocele with Treatment and Prevention Encephalocele is a birth defect in which the brain, its covering, and protective fluid are found outside of the skull. The root cause of an encephalocele is the failure of surface ectoderm to separate from the neuroectoderm early in embryonic development. Complete Information on Encephalitis lethargica with Treatment and Prevention Encephalitis lethargica is an atypical form of encephalitis. The exect cause of encephalitis lethargica is not known for certain. Encephalitis lethargica might be an autoimmune disease, where the body's immune system is triggered by a throat infection (perhaps with a Streptococcus-like bacteria) to attack the nervous system. Complete Information on Emery-Dreifuss muscular dystrophy with Treatment and Prevention Emery-Dreifuss sinewy dystrophy is an uncommon and genetically heterogeneous disorder. The leading reason of mortality and morbidity in emery dreifuss sinewy dystrophy is cardiac disease, which is consistently existing. It usually begins in childhood or adolescence. Complete Information on Elective mutism with Treatment and Prevention Elective mutism is a cultural anxiety disorder in which an individual who is usually able of address is incapable to talk in given situations. No unmarried reason has been established, but there is some evidence that there is a genetic part. Complete Information on Elastosis perforans serpiginosa with Treatment and Prevention Elastosis perforans serpiginosa (EPS) is an uncommon rind disease in which irregular springy tissue fibers, new connective tissue elements, and cellular rubble are expelled from the papillary dermis through the epidermis. Complete Information on Eisenmenger syndrome with Treatment and Prevention Eisenmenger syndrome occurs in patients with big inborn cardiac or surgically created extracardiac left-to-right shunts. These shunts initially induce increased pulmonary blood flowing. Complete Information on Ehrlichiosis with Treatment and Prevention Ehrlichiosis are the general name which is used to describe different bacterial sicknesses which influence animals and people. These sicknesses are caused by the organisms in the type Ehrlichia. Complete Information on Ectrodactyly with Treatment and Prevention Ectrodactyly is an uncommon inborn malformation of the hand where the intermediate digit is missing, and the hand is cleft where the metacarpal of the finger should be. This schism gives the hands the show of lobster claws. Complete Information on Ectopic pregnancy with Treatment and Prevention An ectopic pregnancy is an irregular pregnancy that occurs outside the uterus. Most ectopic pregnancies happen in the fallopian pipe, but implantation can too happen in the cervix, ovaries, and stomach. Complete Information on Ectodermal dysplasia with Treatment and Prevention Ectodermal dysplasia is a disorder involving two or much of the ectodermal structures, which include the rind, hair, nails, teeth, mucus and perspire glands. There are many distinct types of ectodermal dysplasia. Complete Information on Eclampsia with Treatment and Prevention Eclampsia is the occurence of seizures in a pregnant woman. Usually eclampsia occurs after the onslaught of pre-eclampsia though sometimes no pre-eclamptic symptoms are recognisable. Complete Information on Ebstein's anomaly with Treatment and Prevention Ebstein's anomaly is a heart defect in which the tricuspid valve is abnormally formed. In Ebstein's anomaly, two leaflets of the tricuspid valve are displaced downward into the pumping chamber and the third leaflet is elongated and may be adherent to the wall of the chamber. Complete Information on Ebstein's anomaly with Treatment and Prevention Ebstein's anomaly is a heart defect in which the tricuspid valve is abnormally formed. In Ebstein's anomaly, two leaflets of the tricuspid valve are displaced downward into the pumping chamber and the third leaflet is elongated and may be adherent to the wall of the chamber. Complete Information on Bronchiolitis obliterans organizing pneumonia The obliterans of bronchiolite with the pneumonia of organization (BOOP) is an ignition of bronchioles and surrounding fabric in the lungs. BOOP can affect small sectors of the lungs or whole lung. Complete Information on Bronchiolitis obliterans Bronchiolitis obliterans is a rare and life-threatening form of fixed obstructive lung disease in which the bronchioles are plugged with granulation tissue. Complete Information on Brittle bone disease syndrome Brittle bone disease syndrome also known as osteogenesis imperfecta. Osteogenesis imperfecta" means imperfect bone formation. People with this condition have bones that break easily, often from mild trauma or with no apparent cause.
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