- Detailed Information on Moyamoya Disease
Moyamoya illness is a rare, advanced cerebrovascular disorder characterized by the narrowing or occlusion of main blood vessels leading into the brain, and the formation of abnormal blood vessels called moyamoya vessels. - Detailed Information on Mitochondrial Disease
Mitochondrial myopathies are a group of neuromuscular diseases. Mitochondrial diseases result from failures of the mitochondria, specialized compartments present in every cell of the body except red blood cells. - Detailed Information on Mixed Connective Tissue Disease
In Mixed Connective Tissue Disorder, as in other autoimmune diseases parts of the complex immune system is over-active and produces increased amounts of abnormal antibodies that attack the patient's own organs. - Detailed Information on Maple Syrup Urine Disease
Maple Syrup Urine Disease (MSUD) is a disorder abnormally affecting the metabolism of amino acids. The disorder impresses the way the body metabolizes certain components of protein. - Detailed Information on Motor Neuron Disease
Motor neurone disease is one of the most frequent neurodegenerative diseases of adult onset. Motor neurone disease is a advanced, degenerative disorder that affects nerves in the upper or lower parts of the body. - Detailed Information on Medullary cystic disease
Medullary cystic kidney disease is an autosomal dominant kidney disorder characterized by cysts in both kidneys and tubulointerstitial sclerosis leading to end-stage renal illness. - Detailed Information on Ménétrier disease
Ménétrier's disease is also called giant hypertrophic gastritis, protein losing gasteropathy, or hypertrophic gastropathy. Ménétrier's disease increases a person's risk of stomach cancer. - Information on Legionnaire's Disease
Legionnaires' disease is a type of pneumonia. Legionnaires' disease is caused by a type of bacteria called Legionella. The bacteria that reason Legionnaire's disease have been found in water delivery systems and can live in the hot, moist, air conditioning systems of huge buildings, including hospitals. - Information on Ledderhose Disease
Ledderhoses Disease also called morbus ledderhose, plantar fibromatosis and plantar aponeurosis. Ledderhoses Disease is a relatively uncommon non-malignant thickening of the feets deep connective tissue, or fascia. - Information on Krabbe Disease
Krabbe Disease is also known as Globoid Cell Leukodystrophy. Krabbe disease is one of a group of inherited disorders called the leukodystrophies. - Information on Kyrle Disease
Kyrle disease is a rare pathologic condition due to a keratinization disturbance. Kyrle disease is characterized by the formation of large papules with central keratin plugs that may grow in a widespread distribution pattern. - Information on Kohler's Disease
Kohler's disease is an uncommon bone disorder in which the navicular bone of the foot for the time being loses its blood supply (avascular necrosis). It is caused when the navicular bone temporarily loses its blood supply. - Information on Kienbock's Disease
Kienbock's illness is also known as avascular necrosis. Kienbock's illness is a condition in which one of the little bones of the wrist loses its blood supply and dies, causing pain and hardness with wrist movement. - Information on Kikuchi Disease
Kikuchi disease is rare condition. Kikuchi's disease, also called as histiocytic necrotizing lymphadenopathy. Kikuchi's illness is an infection or autoimmune disorder. - Information on Kennedy's Disease
Kennedy's disease, also called is spinal and bulbar muscular atrophy. It is an advanced degenerative condition affecting worse motor neurons. It is one of nine neurodegenerative disorders result by a polyglutamine repeat expansion. - Information on Intervertebral Disc Disease
Intervertebral disk (IVD) disease in the dog is a common clinical disorder manifested by pain, ataxia, paresis, motor paralysis, or sensor motor paralysis. It occurs most often in the chondrodystrophoid dogs but also affects the nonchondrodystrophoid breeds. - Graft versus host disease
Graft-versus-host disease (GVHD) is a common side effect of an allogeneic bone marrow or cord blood transplant (also called a BMT). An allogeneic transplant uses blood-forming cells donated by a family member, unrelated donor or cord blood unit. - Grover's disease
Grover's disease is characterized by an itchy eruption that may last an average of 10-12 months. Grover's disease frequently starts fairly suddenly. It is characterized by papules and papulovesicles with excoriations occurring on the chest, back, lower sternum, arms, and thighs. - Hartnup disease
Hartnup disorder is an inherited metabolic disorder involving the transport of certain amino acids (for example, tryptophan and histidine) in the small intestine and kidneys. - Hallervorden-Spatz disease
Hallervorden-Spatz disease is an inherited, degenerative disease that usually begins in childhood and involves progressive muscle rigidity, weakness, and movement disorder. - Hailey-Hailey disease
Hailey-Hailey disease is also known as familial benign chronic pemphigus. Hailey-Hailey disease is a rare disease of the skin. It can begin at any age, but it is most common in the late teenage years, twenties and thirties. - Gestational trophoblastic disease Detailed Information
Gestational trophoblastic illness is also called a choriocarcinoma. Gestational trophoblastic disease is a quick increasing form of cancer that arises in a woman's uterus after a pregnancy, miscarriage, or abortion. - Graves' disease Detailed Information
Graves' disease is an autoimmune disease characterized by a metabolic imbalance resulting from overproduction of thyroid hormones (thyrotoxicosis). Graves' disease is rarely life-threatening. - Gaucher Disease Detailed Information
Gaucher's disease arises when sure unsafe fatty substances construct to excessive levels in your liver, spleen, lungs, bone marrow and, less normally, your brain. - Freiberg's disease Detailed Information
Freiberg's disease an osteochondrosis affecting the toes: the articular surfaces of the second or third metatarsal heads collapse. It is commonest in girls aged 12-15 years. It causes pain on weight bearing and restricts physical activity. - Fox-Fordyce disease Detailed Information
Fox-Fordyce disease is an rarely happing chronic pruritic papular eruption that place to areas where apocrine glands are create. This condition is also referred to as ‘apocrine duct occlusion’ and ‘sweat retention disease’. - Coeliac Disease Information and Treatment
Coeliac disease is an autoimmune disorder. Celiac disease, also known as celiac sprue. Celiac disease is an inflammatory condition of the tiny intestine precipitated by the ingestion of wheat in individuals with certain genetic makeups. - Buerger's Disease Information and Treatment
Buerger's disease also called as thromboangiitis obliterans. Buerger's disease is an acute inflammation and thrombosis (clotting) of arteries and veins of the hands and feet. Buerger's disease ultimately damages or destroys tissues and may result to infection and gangrene. - Benefits Of Massage Therapy
Massage as a therapeutic instrument has been around for thousands of years in many cultures. Massage is a skilled elixir for better health, but it can too provide a consolidation of system and psyche. - Complete Information on Fascioliasis
Fascioliasis is a foodborne trematode infection that affects patients worldwide causing both liver inflammation and biliary obstruction. Human fascioliasis can be distinguished by an acute and a chronic phase. - Complete Information on Farmer's Lung
Farmer's lung is the most common type of hypersensitivity pneumonitis. Farmer's Lung is a disease caused by breathing in spores from mouldy hay. It affects people who work with hay a lot. - Complete Information on Farmer's Lung
Farmer's lung is the most common type of hypersensitivity pneumonitis. Farmer's Lung is a disease caused by breathing in spores from mouldy hay. It affects people who work with hay a lot. - Complete Information on Farber's Disease
Farber's disease is a rare inherited metabolic disorder. Farber's disease is affected liver, heart, and kidneys. Farber's disease is excess amounts of lipids build up to harmful levels in the joints, tissues, and central nervous system. - Complete Information on Fanconi Anemia
Fanconi anemia is also called nonplastic anaemia. Fanconi anemia is a rare genetic disorder which can be obvious with the birth or during childhood. The anaemia of Fanconi is a predisposition inherited to the gene changes, probably because of a low capacity to repair damage of chromosome. - Complete Information on Familial Mediterranean Fever
Familial mediterranean fever (FMF)) is also called the recurring polyserositis. Family Mediterranean fever (FMF) occurs most generally in the people of the Jewish, Armenian, Arab bottom and Turkish of non-non-ashkenazi. - Complete Information on Familial Adenomatous Polyposis
Familial adenomatous polyposis (FAP) is the syndrome of adénomateux polyposis most common. FAP can affect only 1 in 10.000 people. It is considered a model for the prevention of cancer in the whole world. - Complete Information on Fallot Tetralogy
Tetralogy of fallot is a congenital heart defect. This heart defect is mostly find in children. Congenital heart defects change the normal flow of blood through the heart. This rare and complex heart defect occurs in about 5 out every 10,000 babies. It affects boys and girls equally. - Complete Information on Factor 2 Deficiency
Factor XI (FXI) deficiency is a disorder autosomal which can be associated the bleeding. Factor XI deficiency is a very rare disorder which functions in the families. It has like consequence the weak coagulation of blood. - Complete Information on Fabry Disease
Fabry disease is a X-dependent disease lysosomal recessive of storage. Fabry disease is caused by the lack of or the necessary defective enzyme to metabolize of the lipids, large-like the substances which include oils, waxes, and acids fatty. - Complete Information on Exstrophy of the Bladder
Bladder exstrophy is a congenital defect of birth. Bladder exstrophy is a malformation of the bladder. Bladder exstrophy defect also includes a separation of the pelvic bones. It more often occurs in the boys. - Complete Information on Exercise induced anaphylaxis
Exercise-induced anaphylaxis is a physical form of allergy. Exercise-induced anaphylaxis occurs sometimes only when somebody is exerted within 30 minute to eat certain foods such as corn and of molluscs and shellfish of the anaphylaxis. - Complete Information on Ewing's family of tumors
Ewing's family of tumors (EFT) refers itself to a particular type of tumour which is found in various types of fabric. Ewing's family of tumors also known sarcome of Ewing. - Complete Information on Essential Thrombocytosis
Essential thrombocytosis is chronic disorder myeloproliferative. Myeloproliferative means the not controlled production of the cells by marrow. - Complete Information on Essential Thrombocytopenia
Essential thrombocytopenia is a rare blood disease characterized by the reduced levels of the plates in the blood of circulation. The essential thrombocythemia is one of the diseases myeloproliferative. - Complete Information on Ewing's Sarcoma
Ewing's sarcoma is a cancer. Ewing's sarcoma is a rare disease in which cells of cancer are found in the bone or soft fabric. Ewing's sarcoma usually presents in childhood or the adulthood early, with a peak between 10 and 20 years. - Complete Information on Evan's Syndrome
Evans syndrome is characterized by immunized thrombocytopenia and autoimmune haemolytic anaemia. Autoimmune haemolytic anaemia is a condition in which the red globules which carry oxygen and carbon dioxide normally are destroyed by an autoimmune process. - Complete Information on Esthesioneuroblastoma
Esthesioneuroblastoma, also known olfactory neuroblastoma. Esthesioneuroblastoma is a rare cancer of the higher part of the nasal cavity. It develops in fabric of dependent nerve within the meaning of the odor and can occur in the people of any age. - 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. - 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 . the protoporphyria of Erythropoietic is a relatively soft form of porphyria. - 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 Erythema Nodosum
Erythema nodosum is the clinico pathological alternative most frequent of the panniculitides. Erythema nodosum is an ignition of the large cells under the skin (panniculitis). - 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 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. The pituitary gland is a small gland located at the basis of the brain. - 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. The emphysema is most common among the age 50 people and more old man. Men are affected more often than women. - 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 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. There are many different types of ectodermal dysplasia. - 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 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. The localized character of the disease, while disabling, tends not to be deadly. - 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. - 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 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. Cone-rod dystrophy is too accompanied by amelogenesis imperfecta, an irregularity affecting the teeth. - 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.
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