Clear examples and definition of the Golden Rule. “Do unto others as you would have them do unto you” is the idea (also called the law of reciprocity) that may be. Early life and education. King was born September 21, 1947, in Portland, Maine. His father, Donald Edwin King, was a merchant seaman. King's mother, Nellie Ruth (née. Look, A Punter Highlight. Punters: Are they cool now? Marquette King and the recently retired Pat Mc. Afee have spent the last few seasons trying to convince us that they are, and now they have the support of Bengals punter Kevin Huber. During last night’s preseason game against Washington, Huber turned what should have been a blocked punt into slick highlight: That play was a lot more fun than anything the Jets will do this year. Punters: Are they cool now? Marquette King and the recently retired Pat McAfee have spent the last few seasons trying to convince us that they are, and now they have. What is Eagle? Definition and meaning:EAGLE e'-g'-l (nesher; aetos; Latin aquila): A bird of the genus aquila of the family falconidae. Medical dictionarydisease /dis·ease/ (dĭ- zēz´) any deviation from or interruption of the normal structure or function of any body part, organ, or system that is manifested by a characteristic set of symptoms and signs and whose etiology, pathology, and prognosis may be known or unknown. See also entries under syndrome. ![]() Addison's disease bronzelike pigmentation of the skin, severe prostration, progressive anemia, low blood pressure, diarrhea, and digestive disturbance, due to adrenal hypofunction. Alpers' disease a rare disease of young children, characterized by neuronal deterioration of the cerebral cortex and elsewhere, progressive mental deterioration, motor disturbances, seizures, and early death. Alzheimer's disease progressive degenerative disease of the brain, of unknown cause; characterized by diffuse atrophy throughout the cerebral cortex with distinctive histopathological changes. ASCVD) atherosclerotic involvement of arteries to the heart and to other organs, resulting in debility or death; sometimes used specifically for ischemic heart disease. Ayerza's disease polycythemia vera with chronic cyanosis, dyspnea, bronchitis, bronchiectasis, hepatosplenomegaly, bone marrow hyperplasia, and pulmonary artery sclerosis. Barlow disease scurvy in infants. Binswanger's disease a degenerative dementia of presenile onset caused by demyelination of the subcortical white matter of the brain. United States and Australia, due to Clostridium novyi, marked by necrotic areas in the liver. Bowen's disease a squamous cell carcinoma in situ, often due to prolonged exposure to arsenic; usually occurring on sun- exposed areas of skin. The corresponding lesion on the glans penis is termed erythroplasia of Queyrat. Brill- Zinsser disease mild recrudescence of epidemic typhus years after the initial infection, because Rickettsia prowazekii has persisted in body tissue in an inactive state, with humans as the reservoir. CPDD) an acute or chronic inflammatory arthropathy caused by deposition of calcium pyrophosphate dihydrate (CPPD) crystals in the joints, chondrocalcinosis, and crystals in the synovial fluid. Acute attacks are sometimes called pseudogout. Calvé- Perthes disease osteochondrosis of capitular epiphysis of femur. Canavan disease , Canavan- van Bogaert- Bertrand disease spongy degeneration of the central nervous system. Castleman disease a benign or premalignant condition resembling lymphoma but without recognizable malignant cells; there are isolated masses of lymphoid tissue and lymph node hyperplasia, usually in the abdominal or mediastinal area. Bartonella henselae and characterized by a papule or pustule at the site of a cat scratch, subacute painful regional lymphadenitis, and mild fever. Chagas disease trypanosomiasis due to Trypanosoma cruzi; its course may be acute, subacute, or chronic. Charcot- Marie- Tooth disease muscular atrophy of variable inheritance, beginning in the muscles supplied by the peroneal nerves and progressing to those of the hands and arms. CESD) a lysosomal storage disease due to deficiency of lysosomal cholesterol esterase, variably characterized by some combination of hepatomegaly, hyperbetalipoproteinemia, and premature atherosclerosis. COPD) any disorder marked by persistent obstruction of bronchial air flow. Cf. collagen disorder. Concato's disease progressive malignant polyserositis with large effusions into the pericardium, pleura, and peritoneum. CAD) atherosclerosis of the coronary arteries, which may cause angina pectoris, myocardial infarction, and sudden death; risk factors include hypercholesterolemia, hypertension, smoking, diabetes mellitus, and low levels of high- density lipoproteins. Cowden disease a hereditary disease marked by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Creutzfeldt- Jakob disease a rare prion disease existing in sporadic, familial, and infectious forms, with onset usually in middle life, and having a wide variety of clinical and pathological features. The most commonly seen are spongiform degeneration of neurons, neuronal loss, gliosis, and amyloid plaque formation, accompanied by rapidly progressive dementia, myoclonus, motor disturbances, and encephalographic changes, with death occurring usually within a year of onset. Crigler- Najjar disease see under syndrome. Crohn's disease regional enteritis; a chronic granulomatous inflammatory disease usually in the terminal ileum with scarring and thickening of the wall, often leading to intestinal obstruction and formation of fistulas and abscesses. Cushing's disease Cushing's syndrome in which the hyperadrenocorticism is secondary to excessive pituitary secretion of adrenocorticotropic hormone. In the congenital form, there is hepatosplenomegaly with cirrhosis, and microcephaly with mental or motor retardation. Acquired disease may cause a clinical state similar to infectious mononucleosis. When acquired by blood transfusion, postperfusion syndrome results. Dukes' disease a febrile disease of childhood marked by an exanthematous eruption, probably due to a virus of the Coxsackie- ECHO group. Ebola virus disease fatal acute hemorrhagic fever resembling Marburg virus disease but caused by Ebola virus, seen in the Sudan and Zaire. Ebstein's disease see under anomaly. Fabry's disease an X- linked lysosomal storage disease of glycosphingolipid catabolism resulting from deficiency of α- galactosidase A and leading to accumulation of ceramide trihexoside in the cardiovascular and renal systems. Farber's disease a lysosomal storage disease due to defective ceramidase and characterized by hoarseness, aphonia, dermatitis, bone and joint deformities, granulomatous reaction, and psychomotor retardation. Fazio- Londe disease a rare type of progressive bulbar palsy occurring in childhood. Fox- Fordyce disease a persistent and recalcitrant, itchy, papular eruption, chiefly of the axillae and pubes, due to inflammation of apocrine sweat glands. Freiberg's disease osteochondrosis of the head of the second metatarsal bone. GERD) any condition resulting from gastroesophageal reflux, characterized by heartburn and regurgitation; see also reflux esophagitis. Gaucher's disease a hereditary disorder of glucocerebroside metabolism, marked by the presence of Gaucher's cells in the marrow, and by hepatosplenomegaly and erosion of the cortices of long bones and pelvis. The adult form is associated with moderate anemia and thrombocytopenia, and yellowish pigmentation of the skin; in the infantile form there is, in addition, marked central nervous system impairment; in the juvenile form there are rapidly progressive systemic manifestations but moderate central nervous system involvement. Gilbert disease a familial, benign elevation of bilirubin levels without evidence of liver damage or hematologic abnormalities. Gilles de la Tourette's disease see under syndrome. Iglucose- 6- phosphatase deficiency: a severe hepatorenal form due to deficiency of the hepatic enzyme glucose- 6- phosphatase, resulting in liver and kidney involvement, with hepatomegaly, hypoglycemia, hyperuricemia, and gouttype IB a form resembling type I but additionally predisposing to infection due to neutropenia and to chronic inflammatory bowel disease; due to a defect in the transport system for glucose 6- phosphate. II a disorder due to deficiency of the lysosomal enzyme α- 1,4,- glucosidase, the severe infant form resulting in generalized glycogen accumulation, with cardiomegaly, cardiorespiratory failure, and death, and a milder adult form being a gradual skeletal myopathy that sometimes causes respiratory problems. III a form due to deficiency of debrancher enzyme (amylo- 1,6- glucosidase) in muscle, liver, or both; defects in the liver enzyme are characterized by hepatomegaly and hypoglycemia while defects in the muscle enzyme are characterized by progressive muscle wasting and weakness. IVbrancher enzyme deficiency; cirrhosis of the liver, hepatosplenomegaly, progressive hepatic failure, and death due to deficiency of the glycogen brancher enzyme (1,4- α- glucan branching enzyme). VII muscle weakness and cramping after exercise due to deficiency of the muscle isozyme of 6- phosphofructokinase.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. Archives
November 2017
Categories |