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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 necrotizing ulcerative gingivitis with Treatment and Prevention Acute necrotizing ulcerative gingivitis (ANUG) is a liberal transmission with ulceration, swelling and sloughing away of asleep tissue from the lip and throat payable to the spreading of transmission from the gums. 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. 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. 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. 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. 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. 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°. Complete Information on Costello syndrome Costello syndrome is a rare, distinctive, multiple congenital anomaly syndrome, characterized by soft, loose skin with deep palmar and plantar creases, loose joints, distinctive coarse facial features and skeletal and cardiac abnormalities. Complete Information on Corticobasal degeneration Corticobasal degeneration (CBD) is a progressive neurological disorder. It is associated with atrophy of the cerebral cortex and the basal ganglia. Corticobasal degeneration (CBD) generally occurs in patients age 45 to 70, with women affected more often than men. Complete Information on Conjunctivitis Conjunctivitis commonly known pink Eye. It is an inflammation of the conjunctiva, the clear membrane that covers the white part of the eye and the inner surface of the eyelids. Complete Information on Conversion disorder Conversion disorder is classified as one of the somatoform disorders. Conversion disorder is a psychiatric circumstance in which folk expressed passionate distress through physiological signs and symptoms. Complete Information on Cowden's disease Cowden disease (CD), also known multiple hamartoma syndrome. It is an autosomal dominant condition with variable expression that results most commonly (80%) from a mutation in the PTEN gene on arm 10q, as reported by Liaw et al. Complete Information on Cor triatriatum Cor triatriatum is an inborn eye flaw where the left atrium is subdivided. The membrane divides the correct atrium into a proximal (upper) and a distal (lower) bedroom. Complete Information on Conn's syndrome The Conn comprehensive symptom is the adrenal gland gland disease involves the hormone overproduction. The adrenal gland gland is located above two kidneys the orange decadent internal secretion gland. Complete Information on Congenital torticollis "Congenital" means a condition which is present at the birth. The congenital torticollis occurs or little time after to the birth. This is known as a torticollis muscular congenital. Complete Information on Congenital hepatic fibrosis (CHF) Congenital hepatic fibrosis (CHF) is an uncommon genetic disorder characterized by periportal fibrosis with irregularly shaped proliferating bile ducts, intrahepatic portal hypertension, and esophageal varices. Complete Information on Congenital diaphragmatic hernia Congenital diaphragmatic hernia (too known as CDH) is an irregularity that occurs before birth as a fetus is forming in the mother's womb. Newborns with CDH frequently have serious respiratory distress which can be severe unless treated appropriately. Complete Information on Cytomegalovirus Cytomegalovirus (CMV) is a virus that infects most people worldwide. People are usually infected by the time they are 2 years old or during their teenage years. HCMV infections are frequently associated with salivary glands, though they may be found throughout the body. Complete Information on Congenital amputation Congenital amputation is an inborn disorder caused by fibrous bands of the amnion. This circumstance may be the outcome of the constriction of fibrous bands within the membrane that surrounds the developing fetus or the vulnerability to substances known to induce birth defects (teratogenic agents. Complete Information on Congenital adrenal hyperplasia CAH is a genetic defect of the adrenal glands. People with this condition do no produce enough of the hormones cortisol and aldosterone, and produce too much of androgen. Complete Information on Cone rod dystrophy Cone-Rod Dystrophy (CRD) is an inherited liberal disease that causes worsening of the cone and pole photoreceptor cells and frequently results in blindness. Complete Information on Condyloma Condlyoma is also known wart, genital wart and caused by a virus called the human papilloma virus. The virus is spread by skin-to-skin contact during activity and there does not need to be anal penetration in order to become infected. Complete Information on Compartment syndrome Compartment syndrome is increased tissue pressure within a closed fascial space, resulting in tissue ischemia. Chronic compartment syndrome causes nerve compression and pain, most often in the front of the lower leg. Complete Information on Colpocephaly Colpocephaly is the type forehead is chaotic. This is has the occipital horn one kind of unusual expansion - lateral ventricle behind either rear area the part is chaotic (hole or chamber) the brain. Complete Information on Coloboma Coloboma, also known as keyhole defect of the iris. Coloboma is a congenital genetic disorder. It can appear as a black notch of varying depth at the edge of the pupil, giving the pupil an irregular shape. Complete Information on Colloid cysts Colloid cyst is a cyst containing gelatinous material in the brain. Colloid cysts are relatively rare intracranial lesions located in the rostral aspect of the third ventricle. They may produce acute hydrocephalus, brain herniation, and lead to death. Complete Information on Collagenous colitis Collagenous colitis is called microscopic colitis. Collagenous colitis is a newly-recognized disease of the colon. Complete Information on Coccidioidomycosis Coccidioidomycosis is the transmission caused by the dimorphic fungus Coccidioides immitis. Coccidioides immitis, which is frequently establish in desert regions. Complete Information on Coats disease Coats’ disease also known as exudative retinitis. Coats’ diseas is a rare eye disorder, causing full or partial blindness, characterized by abnormal development of blood vessels behind the retina. Complete Information on Cluttering Cluttering is an address disorder that in many ways is related to stuttering, but is really often distinct than stuttering. Complete Information on Clostridium sordellii Clostridium sordellii is an infrequent human pathogen. It has been demonstrated to be occasionally responsible for myonecrosis or gas gangrene. C. sordellii bacteremia and sepsis occur rarely. Complete Information on Cleidocranial dysplasia Cleidocranial Dysplasia too known as Cleidocranial Dysostosis and characterized by faulty growth of the cranial bones and by the comprehensive or incomplete absence of the leash bones. Complete Information on Churg-Strauss syndrome Churg Strauss syndrome is a type of vasculitis (blood vessel inflammation). Vasculitis diseases are characterized by inflammation of blood vessels. Complete Information on Cerebrospinal fluid leak CSF leak is an escape of the fluid that surrounds the brain and spinal cord. It protects the brain and spinal cord by acting like a liquid cushion. Complete Information on Chronic berylliosis Beryllium disease is an inflammation of the lungs caused by inhaling dust or fumes containing beryllium. Complete Information on Charcot Marie Tooth disease Charcot-Marie Tooth Disease is the most common neuromuscular disease in the world. It is sometimes referred to as "Hereditary Motor and Sensory Neuropathy. Complete Information on Central serous chorioretinopathy Central serous chorioretinopathy too known as Central serous retinopathy (CSR. Central serous chorioretinopathy is a retinal disorder which affects the macula. Complete Information on Chondroectodermal dysplasia Chondroectodermal dysplasia, too known as the Ellis-van Creveld Syndrome. It is an autosomal recessive bony dysplasia that results in short-limbed disproportionate dwarfism. Complete Information on Cutaneous larva migrans Cutaneous larva migrans is the skin manifestation of hookworm infestation. People of all ages, and race can be affected if they have been exposed to the larvae. Complete Information on Cushing's syndrome Cushing's syndrome is a hormonal disorder. Sometimes called "hypercortisolism. Cushing's syndrome is caused by prolonged vulnerability of the system's tissues to higher levels of the hormone cortisol. Complete Information on Cryptosporidiosis Cryptosporidiosis is a disease caused by the parasite Cryptosporidiumparvum. A protozoa infection that usually infects the gastrointestinal tract. Complete Information on Cryptococcosis Cryptococcosis is a rare fungal infection caused by inhaling the fungus Cryptococcus neoformans. Cryptococcus is present around the world, but infection was relatively rare until the AIDS epidemic began. Complete Information on Crohn’s disease The Crohn disease causes the digesting system the inflammation. It the group disease is called the excited intestines disease one by one. Complete Information on Cronkhite-Canada disease Cronkhite Canada disease is an uncommon syndrome. It is characterized by marked epithelial disturbances in the GI parcel and epidermis. Complete Information on Crohn’s disease Crohn's disease is a chronic incendiary disease of the intestines. It primarily causes ulcerations (breaks in the lining) of the tiny and big intestines, but can impact the digestive structure anywhere from the lip to the anus. Complete Information on Crigler Najjar syndrome Crigler-Najjar syndrome (CNS) is a rare autosomal recessive disorder of bilirubin metabolism. This causes jaundice (yellow discoloration of skin and eyes) and organ malfunctions. Complete Information on Cri du Chat syndrome Cri du Chat syndrome also called deletion 5p syndrome. It is a rare genetic disorder due to a missing portion of chromosome 5. Complete Information on Chylous ascites Chylous ascites is a milky-appearing peritoneal fluid that is rich in triglycerides. It is due to the presence of thoracic or intestinal lymph in the abdominal cavity. Complete Information on Cerebellar hypoplasia Cerebellar hypoplasia is a disorder establish in cats and dogs in which the cerebellum is not totally grow at birth. The cerebellum is the part of the mind accountable for the command of movement. When a pup or kitty is born with a developing cerebellum, the circumstance is known as inborn cerebellar hypoplasia. 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 Choroideremia Choroideremia is an uncommon inherited disorder that causes liberal departure of imagination payable to degeneration of the choroid and retina. Choroideremia is a X-linked recessive retinal degenerative disease. Complete Information on Cerebellar ataxia Cerebellar ataxia is a form of ataxia originating in the cerebellum. The cerebellum is part of the brain. It lies under the cerebrum, towards the back, behind the brainstem and above the brainstem. Complete Information on Chagas disease Chagas disease is a transmission caused by the parasite Trypanosoma cruzi. The transmission is normally transmitted via the stool of blood-sucking worm vectors (reduviid bugs. Complete Information on Chronic lymphocytic leukemia The chronic lymphocytic leukemia is the type leukemia. The leukemia either the leukemia are the blood or the marrow cancer and for the unusual proliferation (production description by multiplication) the blood corpuscle. Complete Information on Chronic myelogenous leukemia Chronic myeloid leukemia (CML), too known as chronic myelogenous leukemia. Chronic myelogenous leukemia (CML) is a slow-growing cancer of the light-colored blood cells. Complete Information on Childhood disintegrative disorder Childhood disintegrative disorder (CDD) too known as Heller's syndrome. It's too called dementia infantilis, disintegrative psychosis and pervasive disintegrative disorder. Complete Information on Cervical intraepithelial neoplasia Cervical cancer was the almost popular malignancy in both incidence and mortality. Cervical dysplasia is the irregular increase of cells on the surface of the cervix. Complete Information on Catamenial pneumothorax Catamenial pneumothorax is a rare condition characterized by a reoccurrence of air in the pleural space coinciding with the onset of menses. Complete Information on Cardiospasm Cardiospasm also calls esophagus achalasia and achalasia cardiae. This is chaotic, the esophagus smooth muscle layer weakened wriggled, and the lower esophagus sphincter ill locality relaxed responds swallows down. Complete Information on Cardiomyopathy dilated Dilated cardiomyopathy also known as congestive cardiomyopathy. Dilated cardiomyopathy is a condition of the heart muscle. The heart dilates and pumps blood less well. Complete Information on Carcinoma squamous cell Carcinome of cells of Squamous is the second common cancer of the skin. The cells of Squamous are the small ones, punts cells of skin normally found in the layer external of skin. Complete Information on Carcinoid tumor Carcinoid tumors are an unusual, slow-growing type of cancer that can arise in several places throughout your body. Carcinoid tumor neuroendocrine system is comprised of cells that are spread throughout several organ systems, including the lungs and digestive system. Complete Information on Carcinoid syndrome Carcinoid syndrome is a group of symptoms associated with carcinoid tumor (see bronchial adenoma ). Carcinoid tumors occur most commonly in the gastrointestinal tract, including the stomach, small intestine, appendix, colon and rectum, or in the lungs. Complete Information on Canavan disease The Canavan disease is the aspartic acid metabolism the confusion which inherits. It for degeneration (dispersing) brain white question description. This kind of disease the group gene chaotic is called leukodystrophies one by one. Complete Information on Calciphylaxis Calciphylaxis is a rare, often fatal condition, characterized by progressive cutaneous necrosis that frequently occurs in patients with end-stage renal disease. It is seen almost exclusively in patients with end stage renal disease. Complete Information on Cafe au lait spots Café-au-lait spots are dark spots on the skin that look like birthmarks. Most children have the pigment from birth, and it almost never becomes more extensive. Complete Information on CADASIL Cerebral autosomal predominant arteriopathy with subcortical infarcts and leukoencephalopathy is the almost popular kind of genetic shot disorder. CADASIL is an inherited kind of shot and new impairments. Complete Information on Esophageal atresia with Treatment and Prevention Esophageal atresia, also known as tracheoesophageal fistula, is a agitation of digestive system in which the oesophagus is not developed suitably. This condition takes several different forms, often involving one or more fistulas connecting the trachea to the esophagus. Complete Information on Erythropoietic protoporphyria with Treatment and Prevention Erythropoietic protoporphyria (EPP) is a group's member disease calls porphyrias. The protoporphyria of erythropoietic usually begins in infancy, even if there is a shape of in delay-beginning that in the first place happens when the person is an adult. Complete Information on Erythromelalgia with Treatment and Prevention Erythromelalgia, also known under the name of disease of the mitchell, neuralgia red, or erythermalgia, is a rare disorder in which blood vessels, usually in the lower ends, are episodically blocked and inflamed. Complete Information on Erythema multiforme with Treatment and Prevention Erythema multiforme (EM) is an intense, self-limiting, incendiary rind outbreak. It is a character of hypersensitive response that occurs in reaction to medications, infections, or sickness. The precise reason is unidentified. Complete Information on Erythema elevatum diutinum with Treatment and Prevention Erythema elevatum diutinum is a chronic and uncommon dermatosis that is considered to be a variation of leukocytoclastic vasculitis. The exect reason of erythema elevatum diutinum is unidentified, although the pathogenesis is believed to be exempt complex-mediated. Complete Information on Erysipelas with Treatment and Prevention Erysipelas is a trivial transmission of the rind, which typically involves the lymphatic structure. This disease is too known as saint anthony's flame. This disease is almost popular among the older, infants, and children. Complete Information on Erdheim chester syndrome with pyloric atresia with Treatment and Prevention Erdheim-Chester disease is an uncommon kind of non-Langerhans-cell histiocytosis. The disease involves an infiltration of lipid-laden macrophages, multinucleated large cells, an incendiary penetrate of lymphocytes and histiocytes in the ivory marrow, and a generalized sclerosis of the lengthy bones. Complete Information on Epidermolysis bullosa acquisita with Treatment and Prevention Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal blistering disease of the rind and mucus membranes. It is a chronic incendiary disease with periods of incomplete remissions and exacerbations. Complete Information on Epidermolysis bullosa with Treatment and Prevention Epidermolysis bullosa (EB) is a group of inherited bullous disorders. Infancy is a particularly hard moment for epidermolysis bullosa patients. Generalized blistering caused by any subtype may be complicated by transmission, sepsis, and death. Complete Information on Cerebral aneurysm or brain aneurysm Cerebral aneurysms, also called intracerebral. Cerebral aneurysms are abnormal saccular outpouchings of blood vessels occurring on blood vessels of the brain. 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.
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