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Complete Information on Cold agglutinin disease Cold Agglutinin Disease, a rare blood disorder, is a type of autoimmune hemolytic anemia. Cold agglutinin disease, also called cold antibody disease. Cold agglutinin disease (CAD) usually develops as a result of the production of a specific IgM antibody directed against the I/i antigens (precursors of the ABH and Lewis blood group substances) on RBCs. Complete Information on Cogan's syndrome Cogan's syndrome is an uncommon, rheumatic disease characterized by inflammation of the ears and eyes. Cogan’s syndrome causes symptoms that are related to those of syphilic keratitis although there is no evidence of pox transmission in Cogan’s syndrome. Complete Information on Cohen syndrome Cohen Syndrome is an uncommon hereditary disorder caused by a recessive gene. Cohen Syndromeis characterized by childish hypotonia (a weakening of the bony muscles), childhood obesity, and several malformations. Complete Information on Coffin-Siris Syndrome The coffin Siris synthesis symptom is the rare gene abnormality. Perhaps chaotic for feeds the description difficult and the frequent breath infection in the initial period, the muscle which reduces is been anxious (hypotonia), the unusual looseness (laxity) joins, bone age which retards, with intelligence flaw period. Complete Information on Cockayne syndrome Cockayne syndrome is a rare inherited disorder in which people are sensitive to sunlight, have short stature and have the appearance of premature aging. Cockayne syndrome can be shared into subtypes, which are distinguished by the severity and age of onset of symptoms. Complete Information on Coal worker's pneumoconiosis Coal worker's pneumoconiosis is a lung disease caused by breathing in debris from coal, graphite, or synthetic carbon for a lengthy moment. CWP normally causes no symptoms but can advance to liberal big fibrosis with diminished lung role. Complete Information on Cat Scratch Disease Cat scratch disease (CSD) is a bacterial disease caused by Bartonella henselae. The bacteria can be passed from a cat to a human. Most people with CSD have been gnawed or scratched by a cat and developed a mild infection at the point of injury. Complete Information on Castleman's disease Castleman's disease is an uncommon lymphoproliferative disorder. It is characterized by non-cancerous (benign) growths (tumors) that may develop in the lymph node tissue throughout the body. It involves hyperproliferation of certain B cells that often produce cytokines. Complete Information on Cartilage-hair hypoplasia Cartilage-hair hypoplasia is an autosomal recessive inherited disorder. Cartilage-hair hypoplasia (CHH) is a kind of short-limbed dwarfism payable to bony dysplasia. Cartilage-hair hypoplasia and new short-limb dwarfism phenotypes are associated with metaphyseal or spondyloepiphyseal dysplasia. Complete Information on Carpenter syndrome Carpenter's syndrome is an exceedingly uncommon craniofacial disorder. Carpenter syndrome belongs to a group of uncommon hereditary disorders. Carpenter syndrome is known as acrocephalopolysyndactyly (ACPS) disorders. Complete Information on Caroli disease Caroli disease also is known as communicating cavernous ectasia. Caroli's disease is a rare inherited disorder of the liver. It is characterized by saccular and cystic dilatation of intra-hepatic biliary ducts. Complete Information on Carney syndrome Carney's syndrome is considered unusual autosomal dominantly transmitted multisystem tumorous disorder. It is characterized by myxomas , uneven rind pigmentation , endocrine tumors , and incidental heart tumors (schwannomas. Approximately 150 affected patients are known global. Complete Information on Caffey disease Caffey disease also known infantile cortical hyperostosis. The main feature of the disease is a peculiar cortical thickening of certain bones like the mandible, the clavicles, and the shafts of long bones. Complete Information on Eosinophilic granuloma with Treatment and Prevention Eosinophilic granuloma is a condition reserved for the almost frequently and harmless kind of disorder known as Langerhans cells histiocytosis. Eosinophilic granuloma is a harmless disorder that affects children and inexperienced adults, especially males. Complete Information on Eosinophilic fasciitis with Treatment and Prevention The eosinophilic fasciitis is a disorder idiopathic and fibrotic with the seal histopathologic of the fibrosis fascial. The causes is unknown, but aberrant immune responses may play a role because hypergammaglobulinemia and antinuclear antibodies are associated. Complete Information on Eosinophilia-myalgia syndrome with Treatment and Prevention Eosinophilia myalgia syndrome (EMS) is an uncommon, multi-systemic, and chronic autoimmune disease caused by ingestion of impure L-tryptophan. It can impact any system structure, such as pulmomary, gastro-intestinal or the skin. Complete Information on Ehlers-Danlos syndrome with Treatment and Prevention Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that undermine connective tissues. Depending on the private variation, the hardship of the disease can change from balmy to severe. There are six leading types of Ehlers danlos syndrome. Complete Information on Edwards syndrome with Treatment and Prevention Edwards syndrome is a hereditary disorder. It is the almost popular autosomal trisomy after Down Syndrome that carries to term. Edwards' syndrome is caused by an additional transcript of chromosome 18. For this cause, it is too called trisomy 18 syndrome. Complete Information on Brown-Sequard syndrome Braun the Sequard synthesis symptom (BSS) is a rare neurology situation. It in causes weakness or the paralysis spinal cord for the harm description (hemiparaplegia) (hemianesthesia) loses in the bodily one side and the feeling in the reverse side. Complete Information on Budd-Chiari syndrome Budd-Chiari syndrome is clotting of the hepatic vein, the major vein that leaves the liver. Budd-Chiari syndrome usually occurs when a clot narrows or blocks the hepatic veins. The acute syndrome presents with rapidly progressive: severe upper abdominal pain, jaundice, hepatomegaly (enlarged liver), ascites, elevated liver enzymes, and eventual encephalopathy. Complete Information on Brugada syndrome Brugada syndrome is a genetic disorder in which an abnormality in the heart's electrical system causes life-threatening heart rhythm disturbances (arrhythmiasBrugada syndrome is characterized by ST-segment abnormalities in leads V1-V3 on ECG and a high risk of ventricular arrhythmias and sudden death. Complete Information on Burkitt's lymphoma Burkitt lymphoma is a cancer of the lymphatic structure. Burkitt’s lymphoma usually affects children. Burkitt's is uncommon; boys are more possible to get lymphomas of any character than girls. Complete Information on Boerhaave syndrome Boerhaave syndrome is a rare spontaneous rupture to the esophagus. Esophagus most commonly results from a sudden increase in intraesophageal pressure combined with negative intrathoracic pressure caused by straining or vomiting. Complete Information on Birt-Hogg-Dube syndrome Birt-Hogg-dubé syndrome (BHD) is a very rare human genetic disorder. It is characterized by hair follicle hamartomas, kidney tumors, and spontaneous pneumothorax. Complete Information on Bilateral renal agenesis Bilateral Renal Agenesis is a hereditary disorder characterized by a bankruptcy of the kidneys to produce in a fetus. This absence of kidneys causes an inadequacy of amniotic fluid in a pregnant woman. This disorder is more popular in infants born of a parent who has a kidney deformity, especially the absence of one kidney. Complete Information on Bietti's crystalline dystrophy Bietti's lucid dystrophy (BCD) is uncommon inherited heart disease characterized by crystals in the clear-cut coating of the heart. The symptoms of BCD include: crystals in the cornea ; yellow, glossy deposits on the retina; and liberal wasting of the retina, choriocapillaries and choroid. Complete Information on Beckwith-Wiedemann syndrome Beckwith-Wiedemann Syndrome (BWS) is a congenital overgrowth syndrome, which can affect all systems of the body. It is associated with an elevated risk of embryonic tumor formation. Complete Information on Barre Lieou syndrome A syndrome characterized by trauma or arthritic changes involving the third and fourth cervical vertebrae or cervical disk lesions with provocation of the cranial nuclei, the fifth and eight cranial nerves being chiefly affected. Complete Information on Bare lymphocyte syndrome Bare lymphocyte syndrome is a disease resulting from severely receded gene conditions. Bare lymphocyte syndrome, which results from deficiencies in the major histocompatibility complex, is broken down into Type 1 and Type 2. Complete Information on Barakat syndrome Barakat syndrome, also known as HDR syndrome. Barakat syndrome (medical condition) is characterized by deafness, kidney disease and insufficiency parathyroid hormone production. Complete Information on Banti's syndrome Banti's Syndrome, also known as Banti's disease, is an illness characterized by an enlargement of the spleen with anemia. These terms were actually used more in the past then they are today. Complete Information on Balo disease with Treatment and Prevention Balo's disease is a rare progressive form of multiple sclerosis with a strong viral association that primarily affects young adults. Multiple Sclerosis (MS) is an instigative disease of the Central Nervous System (CNS). Predominantly, it is a disease of the "white matter" tissue. Complete Information on Duchenne muscular dystrophy with Treatment and Prevention Duchenne sinewy dystrophy is a hereditary disorder that gradually weakens the system's muscles. This disorder is caused by a variation in a particular gene within the X chromosome that provides instructions for the establishment of the dystrophin protein, a significant structural part of muscle tissue. Complete Information on Dubowitz syndrome with Treatment and Prevention Dubowitz syndrome is a genetic disorder defined by slow growth, a characteristic facial appearance, and a small head. Although the exact pathology of Dubowitz syndrome is not yet known, it is almost certain that it has a genetic component. Complete Information on Dubin-Johnson syndrome with Treatment and Prevention Dubin-Johnson syndrome (DJS) is a character of genetic hyperbilirubinemia which causes a growth of conjugated bilirubin without altitude of liver enzymes. This circumstance is associated with a flaw in the power of hepatocytes to secrete conjugated bilirubin into the bile. Complete Information on Digeorge syndrome with Treatment and Prevention Digeorge syndrome is a disorder gift at inborn, caused by problems within a developing embryo that happen payable to chromosome defects. It is too called thymic aplasia, thymic hypoplasia, or third and fourth pharyngeal archway or pocket syndrome. Complete Information on Demyelinating disease with Treatment and Prevention A demyelinating disease is any circumstance that results in harm to the overprotective coating that surrounds nerves in your mind and spinal cord. This impairs the conduction of signals in the affected nerves, causing disability in superstar, campaign, cognition, or new functions depending on which nerves are involved. Complete Information on Degos disease with Treatment and Prevention Degos disease, too known as cancerous atrophic papulosis, causes clogging of tiny and cooked size arteries in the system. The reason of Degos disease and how it develops in the system are unidentified. Complete Information on De Quervains' disease with Treatment and Prevention De Quervain's disease is a term used to describe a painful disorder affecting the tendons at the base of the thumb. Often, the cause is unknown, but overuse, a direct blow to the thumb, repetitive grasping, and certain inflammatory conditions such as rheumatoid arthritis can all trigger the disease. Complete Information on Darier's disease with Treatment and Prevention Darier's disease is an autosomal dominantly inherited genodermatosis. The principal reason of this disease is irregularity in the gene, environmental factors, warmth, humidity, and vulnerability to sunshine. Complete Information on Dandy walker syndrome with Treatment and Prevention Dandy-Walker Syndrome is an inborn mind deformity involving the cerebellum (a region at the rear of the mind that controls campaign) and the fluid filled spaces around it. Parents of children with nifty walker syndrome may gain from hereditary guidance if they mean to get much children. Complete Information on Auditory neuropathy with Treatment and Prevention Auditory neuropathy is a hearing disorder in which audio enters the inner ear usually but the infection of signals from the inner ear to the mind is impaired. An individual with auditory neuropathy may be capable to learn sounds, but would yet get trouble recognizing spoken words. Complete Information on Atypical mole syndrome with Treatment and Prevention Atypical Mole Syndrome is a genetic circumstance which causes the individual to get a big amount of moles with some dysplastic nevi. This frequently leads to a high danger of melanoma, a severe rind cancer. Complete Information on Atypical hemolytic uremic syndrome with Treatment and Prevention Atypical hemolytic uremic syndrome (AHUS) is an exceedingly uncommon group of disorders of the kidneys. It is a clearly distinct sickness from hemolytic uremic syndrome. The syndrome is not caused by a foreign broker (such as a bacterium, virus etc). Complete Information on Aspartylglycosaminuria with Treatment and Prevention Aspartylglycosaminuria (AGU) are ingeboren an error of metabolism which is caused by inadequate activity of the enzyme aspartylglucosaminidase. It occurs as a result of deficient activity of a particular enzyme, leading to the accumulation of metabolic products in the body. Complete Information on Asherman's syndrome with Treatment and Prevention The syndrome of Asherman is stipulated by the presence of intrauterine permanent adherence, which erases or entirely the uterus cavity partially. Most commonly, intrauterine adhesions occur after a dilatation and curettage that was performed because of a miscarriage or because of retained placenta with or without hemorrhage after a delivery. Complete Information on Apert syndrome with Treatment and Prevention The Apert symptom is a gene slight defect and belongs to the craniofacial anomaly the broad classification. The chances of having another child with Apert Syndrome is almost non-existent if both parents are unaffected. If one parent has Apert Syndrome, there is a chance that his children will have Apert Syndrome. Complete Information on Aortic supravalvular stenosis with Treatment and Prevention Aortic supravalvular stenosis is a fixed kind of inborn left ventricular leakage parcel interference that occurs as a localized or a diffuse narrowing of the ascending aorta beyond the excellent edge of the sinuses of Valsalva. Complete Information on Aortic coarctation with Treatment and Prevention Aortic coarctation is a narrowing of region of the aorta. The aorta carries blood from the eye to the vessels that provide the system with blood and nutrients. If region of the aorta is narrowed, it is difficult for blood to give through the artery. Complete Information on Aortic arch interruption with Treatment and Prevention Interruption of the aortic archway is an uncommon and normally deadly inborn anomaly that is frequently associated with dual cardiac malformations. It is normally occurs in association with a nonrestrictive ventricular septal flaw and ductus arteriosus or, less usually, with a big aortopulmonary window or truncus arteriosus. Complete Information on Antisocial personality disorder with Treatment and Prevention Antisocial personality disorder is a condition in which people show a pervasive disregard for the law and the rights of others. Basic characteristic which considered chaotic is the deceit and the operation. Complete Information on Antiphospholipid syndrome with Treatment and Prevention The syndrome of Antiphospholipid is a disorder of the coagulation, which causes clots of blood in arteries and veins, as well as of the complications connected by pregnancy like loss, serious delivery of preterm, or preeclampsia. Complete Information on Angelman syndrome with Treatment and Prevention The Angelman synthesis symptom is affects the nervous system the complex gene to be chaotic. AS is a classic example of genetic imprinting caused by deletion or inactivation of critical genes on the maternally inherited chromosome. Complete Information on Androgen insensitivity syndrome with Treatment and Prevention Androgen insensitivity syndrome is a range disorder of sexual differentiation which results from changes of the gen that the androgen encode sensor. It has also been called androgen resistance in the medical literature. Complete Information on Andersen Tawil syndrome with Treatment and Prevention Andersen tawil syndrome is a rare genetic disorder, its occurrence is unknown. Anderson the tawil synthesis symptom is causes the periodic paralysis plot the confusion, change in heart rhythm, with development abnormality. Complete Information on Amyloid angiopathy with Treatment and Prevention Amyloid angiopathy is too known as congophilic angiopathy or cerebrovascular amyloidosis. Amyloid angiopathy may impact patients over age 45, but is almost popular in patients over age 65, and becomes more popular with increasing age. Complete Information on Amniotic band syndrome with Treatment and Prevention Amniotic band syndrome is an inborn disorder caused by entrapment of fetal parts (normally an arm or digits) in fibrous amniotic bands while in utero. The amniotic ring hypothesis is that ABS occurs payable to an incomplete rift of the amniotic sac. Complete Information on Alveolar soft part sarcoma with Treatment and Prevention Alveolar soft part sarcoma (ASPS) is a malignant soft tissue tumor that has an unclear origin. The term sarcoma assign to malignant tumors of tissues that connect, support, or surround other structures and organs of the body such as bone, cartilage, fat, muscle. Complete Information on Alveolar echinococcosis with Treatment and Prevention Alveolar echinococcosis is a chronic disease with a presymptomatic phase that may live for years before signs and symptoms produce. The variance of the signs and symptoms depends on the position of the lesions, which may produce in the liver and in respective organs or tissues, particularly the lungs, mind, and bones. Complete Information on Alternating hemiplegia of childhood with Treatment and Prevention Alternating hemiplegia is an uncommon neurological disorder that develops in childhood. The disorder is characterized by regular, short-lived episodes of paralysis on one position of the system. Complete Information on Alstrom syndrome with Treatment and Prevention Alstrom syndrome is an acquired disorder marked by blindness, deafness, diabetes, and obesity. This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Complete Information on Alport syndrome with Treatment and Prevention Alport syndrome is an acquired disorder that leads to kidney damage. In Alport syndrome, type IV collagen, one of the proteins that makes up the GBM, is absent or abnormal. Most people with Alport syndrome develop kidney failure in early adult life - in their late teens or twenties. Complete Information on Allergic bronchopulmonary aspergillosis with Treatment and Prevention Allergic bronchopulmonary aspergillosis is a hypersensitive lung response to a fungus called aspergillus, which causes inflammation of the airways and atmosphere sacs of the lungs. The fungus Aspergillus fumigatus flourishes in land, decaying flora, foods, dusts, and water. Complete Information on Allan-Herndon-Dudley syndrome with Treatment and Prevention Allan herndon dudley syndrome is an uncommon disorder of mind growth that causes conservative to serious psychological retardation and problems with campaign. This circumstance, which occurs solely in males, disrupts growth from before birth. Complete Information on Aicardi-Goutieres syndrome with Treatment and Prevention Aicardi-Goutieres syndrome is inherited in an autosomal recessive manner. Aicardi-Goutieres Syndrome is mostly either fatal, or else it results in a persistent vegetative state in early childhood. Complete Information on Aicardi syndrome with Treatment and Prevention Aicardi syndrome is an uncommon hereditary disorder, characterized by the incomplete or comprehensive absence of the system that links the two hemispheres of the mind, the corpus callosum. Complete Information on Agnosia with Treatment and Prevention Agnosia is a departure of power to know objects, persons, sounds, shapes, or smells while the particular sense is not faulty nor is there any substantial memory departure. Agnosia can ensue from strokes, dementia, or new neurological disorders. Complete Information on African trypanosomiasis with Treatment and Prevention African trypanosomiasis, also known as sleeping sickness, is a sober tropical disorder that is always deadly without treatment. There are two types of african trypanosomiasis, named for the regions in africa in which they are found: East african trypanosomiasis and west african trypanosomiasis. Complete Information on Burning mouth syndrome Burning mouth syndrome (BMS) is a condition that causes pain in the mouth, lips or tongue without any clear reason. There are often no visible signs of irritation. The cause of the syndrome may be caused by the onset of menopause to vitamin deficiencies. Complete Information on Bullous pemphigoid Bullous pemphigoid normally occurs in older persons and is uncommon in inexperienced folk. Bullous pemphigoid is a rind disease characterized by uneasy blistering eruptions on the surface of the rind. Complete Information on Buerger's disease Buerger's disease, too known as thromboangiitis obliterans. Buerger's disease is an uncommon and incendiary disorder affecting incidental blood vessels and resulting in pain, ulceration, thrombosis and Raynaud's phenomenon. Complete Information on Brown syndrome Brown's syndrome, also called superior oblique tendon sheath syndrome. Brown Syndrome is a rare eye disorder characterized by defects in eye movements. It involving fibrous adhesions in the upper medial quadrant of the orbit. Complete Information on Brucellosis The brucelosis also called fever undulant. The brucelosis is a bacterial disease that can affect any organ of the body. One is through the world. The brucelosis is a disease mainly of cattles, pigs, goats, ewes and dogs. Complete Information on Bronchogenic cyst Bronchogenic cysts is almost popular cystic lesion of the mediastinum. The cysts are normally establish using antenatal sonography and regular chest radiography and during evaluations for GI or cardiac symptomatology. Complete Information on Bright’s Disease Bright's disease, or nephritis, an inflammation of the filtering units in the kidneys. It is typically denoted by the presence of serum albumin in the urine, and frequently accompanied by edema. Complete Information on Brain tumor Brain is a tender, soft people of tissue. It is protected by the bones of the skull and three slim membranes called meninges. Cancer begins in cells, the construction blocks that take upward tissues. Complete Information on Bradykinesia Bradykinesia is one of the constituents of Parkinson's disease. Bradykinesia is a movement disorder and a perception disorder. Bradykinesia Slowed power to begin and remain movements, and diminished power to adapt the system's stance. Complete Information on Bradykinesia Bradykinesia is one of the constituents of Parkinson's disease. Bradykinesia is a movement disorder and a perception disorder. Bradykinesia Slowed power to begin and remain movements, and diminished power to adapt the system's stance. Complete Information on Brachyolmia Brachyolmia is a rare form of skeletal dysplasia. Brachyolmia is a form of spondylodysplasia. It is characterized by generalized platyspondyly without significant epiphyseal, metaphyseal, or diaphyseal changes in the long bones. Complete Information on Brachydactyly BD is usually isolated, meaning that it is not associated with any other medical problems. Brachydactyly (BD) refers to shortening of the fingers or toes due to underdevelopment of the bones in the hands or feet. Complete Information on Bowen's disease Bowen's disease is also called squamous cell carcinoma. It is a form of skin cancer. Bowen’s disease is a growth of abnormal cells that is confined to the outer layer of the skin. Complete Information on Botulism Botulism is a paralytic disease caused by the neurotoxins of Clostridium botulinum. In the United States an average of several cases of botulism are reported each year. Of these, approximately 25% are foodborne, 72% are infant botulism, and 3% are wound botulism. Complete Information on Borreliosis Borreliosis are a contagion and cause by bit of a tik which is contaminated with bacteria Lyme. Burgdorferi of Borrelia the name of the bacteria has been most generally linked to borreliosis. Complete Information on Blue rubber bleb nevus Blue rubber bleb nevus syndrome is a rare disorder that consists mainly of abnormal blood vessels affecting the gastrointestinal tract. It is even a rare cause of gastrointestinal hemorrhage during childhood. Complete Information on Blue diaper syndrome Blue diaper syndrome is a rare, autosomal recessive metabolic disorder characterized in infants by bluish urine-stained diapers.Blue diaper syndrome is an inborn error of amino acid metabolism. Complete Information on Blount disease Blount's disease is a growth disorder of the tibia (shin bone) that causes the lower leg to angle inward, resembling a bowleg. Blount's Disease is one which affects the bone development of toddlers and older children. Complete Information on Bloom syndrome Bloom syndrome is a rare inherited illness characterized by a high frequency of breaks and rearrangements in an affected person's chromosomes. Bloom syndrome is a very rare disorder in most populations. Complete Information on Blood coagulation disorders Blood coagulation is part of an important host defense mechanism termed hemostasis. Upon vessel injury, platelets adhere to macromolecules in the subendothelial tissues and then aggregate to form the primary hemostatic plug. Complete Information on Blepharospasm Blepharospasm is an abnormal, involuntary blinking or spasm of the eyelids. Benign essential blepharospasm (BEB) is the most common type of blepharospasm. Blepharospasm is a type of dystonia. Complete Information on Birdshot chorioretinopathy Birdshot chorioretinopathy is heart disorder where the heart has an amount of light-colored specks around the optic disc payable to an inflammation inside the heart. Birdshot chorioretinopathy occurs predominantly in inexperienced adults, with a nasty age of onslaught of 27 years. Complete Information on Blastomycosis Blastomycosis is an uncommon, but potentially serious fungal infection. Blastomycosis is an infection found in dogs, people, and occasionally cats. It primarily affects the lungs and skin. It is caused by Blastomyces dermatitidis. Complete Information on Biotinidase deficiency Biotinidase Deficiency (BIOT) is caused by the lack of an enzyme called biotinidase. This disorder is classified as a multiple carboxylase deficiency, a group of disorders characterized by impaired activity of certain enzymes that depend on biotin. Complete Information on Binswanger's disease Binswanger's disease (BD), also called subcortical vascular dementia. Binswanger's disease is a rare form of dementia characterized by cerebrovascular lesions in the deep white-matter of the brain, loss of memory and cognition, and mood changes. Complete Information on Biliary cirrhosis Primary biliary cirrhosis (PBC) is a disease characterized by incendiary devastation of the tiny bile ducts within the liver. PBC finally leads to cirrhosis of the liver. PBC has a global prevalence of roughly 5/100,000 and a yearly incidence of roughly 6/1,000,000. Complete Information on Biliary atresia Biliary Atresia is a rare gastrointestinal disorder. Biliary atresia is characterized by obliteration or discontinuity of the extrahepatic biliary system, resulting in obstruction to bile flow. Complete Information on Bile duct cysts Bile duct cysts also called is choledochal cysts. This a congenital abnormality of the bile duct that causes abnormal enlargement of the bile duct. Bile duct cysts are rare and of uncertain origin. Complete Information on Bile duct cancer Bile duct cancer is a type of liver cancer, in which malignant (cancerous) tumours grow in the bile ducts. It is also known as cholangiocarcinoma and is rare in the UK, only accounting for approximately 1% of cancers in the UK. Complete Information on Bile acid synthesis defect Bile acids are chemicals made by the liver and put into bile, the yellow fluid that flows from the liver to the intestines. Bile acids are the body's natural detergents that help the intestine lose it and use the fat and vitamins from the foods we eat. Complete Information on Beta ketothiolase deficiency Beta-ketothiolase inadequacy in a household confirmed by in vitro enzymatic assays in fibroblasts. Metabolism is the procedure your system uses to have or have vitality from the nutrient you consume. Complete Information on Beta-thalassemia Beta-thalassemia also known as Cooley's anemia. Beta-thalassemia happens when the body is unable to make an important blood protein called beta globin. Beta-thalassemia is caused by abnormalities in the beta-globin gene, located on chromosome 11.
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