HealthCentral - General Encyclopedia - Crigler-Najjar Syndrome General Health Encyclopedia, criglernajjar syndrome. Causes, incidence, and risk factors crigler-najjar syndrome is inherited as an autosomal recessive trait. http://www.healthcentral.com/mhc/top/001127.cfm
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Extractions: Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Crigler-Najjar Syndrome Austin Health Information - An overview of crigler-najjar syndrome including symptoms, treatment and prevention. Conditions and Diseases - Crigler-Najjar Syndrome Top Links - Crigler-Najjar Syndrome Web Site Links. HealthCentral - General Encyclopedia - A look at crigler-najjar syndrome including, the symptoms Crigler Najjar Syndrome Type I,Bilirubin Glucuronosyltransferase ... - Crigler Najjar Syndrome Type I,Bilirubin Glucuronosyltransferase Deficiency Type I,Uridine Diphosphate Glucuronosyltransferase Severe Def. Crigler-Najjar Disease - Bi-lingual site with information and links on this disease. Crigler-Najjar syndrome - Crigler-Najjar syndrome. Glucuronyl transferase deficiency (type I); Arias syndrome (type II Crigler-Najjar). Causes, incidence, and risk factors: CRIGLER-NAJJAR SYNDROME - CRIGLER-NAJJAR SYNDROME - A rare genetic defect (autosomal recessive) where there is the inability to form bilirubin glucuronide due to the absence of the Crigler-Najjar Syndrome - Crigler-Najjar Syndrome Directory: Guide to Crigler-Najjar Syndrome sites on the internet. Crigler-Najjar Syndrome.
ORPHANET® Crigler-Najjar Syndrome ORPHANET. Orphanet database access. criglernajjar syndrome. Direct access to data Summary crigler-najjar syndrome is a very rare disease http://www.orpha.net/static/GB/criglernajjarsyndrome.html
Crigler-Najjar, Syndrome : Sites Et Documents Francophones Translate this page Crigler-Najjar, syndrome. Menu général CISMeF. Arborescence(s) du thesaurus MeSH contenant le mot-clé Crigler-Najjar, syndrome crigler-najjar syndrome http://www.chu-rouen.fr/ssf/pathol/criglernajjarsyndrome.html
Extractions: Crigler-Najjar, syndrome Menu général CISMeF Définition [MeSH Scope Note ; traduction CISMeF] : Forme familiale d'hyperbilirubinémie congénital transmise autosomale récessive. Elle est caractérisée par un ictères et des lésions cérébrales provoquées par une insuffisance en glucuronyl transférase dans le foie et la conjugaison défectueuse de la bilirubine.
Health Library - criglernajjar syndrome type I is inherited as an http//www.PICKonline.org Crigler-Najjar Association 3134 mauckc@msn.com Internet www.criglernajjar.com. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw
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Genetic Disorders, Crigler-Najjar Syndrome Category Home Health Conditions and Diseases Genetic Disorders criglernajjar syndrome. * Site Title · The name of the site. http://www.iseekhealth.com/directory/index.php?method=show_link_exchange&directo
Extractions: Related links of interest: An inherited disorder of bilirubin metabolism in which bilirubin cannot be changed into its water-soluble form, bilirubin glucuronide. This is caused by an enzyme imbalance in the liver. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the Open Directory and has been modified and enhanced using our own technology.
Extractions: Back Back to main Health Information page Liver anatomy Definition: Crigler-Najjar syndrome is an inherited disorder in which bilirubin (a substance made by the liver) cannot be changed into its water-soluble form, bilirubin glucuronide. This causes jaundice (yellow discoloration of skin and eyes) and organ malfunctions. Alternative Names: Glucuronyl transferase deficiency (type I Crigler-Najjar); Arias syndrome (type II Crigler-Najjar) Causes And Risk: Crigler-Najjar syndrome is caused by an abnormal gene which fails to produce a functional enzyme (bilirubin glucuronyltransferase) capable of converting bilirubin into a water-soluble and therefore, easily excreted form. As a result, bilirubin can build up in the body, which can damage the brain and other organs. The syndrome is inherited as an autosomal recessive trait. This means that the child must get the defective gene from both parents to develop the severe form of the condition. Parents who are carriers (with just one defective gene) have about half the normal enzyme activity of a normal adult. Infants who inherit the trait from both parents (this is called homozygous for the abnormal gene) develop severe jaundice (hyperbilirubinemia) beginning a few days after birth. If these infants are not treated, they may develop
Crigler-Najjar Syndrome criglernajjar syndrome. Definition Alternative Names Glucuronyl transferase deficiency (type I Crigler-Najjar); Arias syndrome (type II Crigler-Najjar). http://www.drkoop.com/ency/article/001127.htm
Extractions: Advertisement Disease Injury Nutrition Poison ... Prevention Definition: Crigler-Najjar syndrome is an inherited disorder in which bilirubin (a substance made by the liver) cannot be changed into its water-soluble form, bilirubin glucuronide. This causes jaundice (yellow discoloration of skin and eyes) and organ malfunctions. Causes, incidence, and risk factors: Crigler-Najjar syndrome is caused by an abnormal gene which fails to produce a functional enzyme (bilirubin glucuronyltransferase) capable of converting bilirubin into a water-soluble and therefore, easily excreted form. As a result, bilirubin can build up in the body, which can damage the brain and other organs. The syndrome is inherited as an autosomal recessive trait. This means that the child must get the defective gene from both parents to develop the severe form of the condition. Parents who are carriers (with just one defective gene) have about half the normal enzyme activity of a normal adult.
Crigler-Najjar Syndrome criglernajjar syndrome. Liver biopsy, enzyme assay for low-absent Glucuronyl transferase activity; A family history of crigler-najjar syndrome. http://www.drkoop.com/ency/article/001127sym.htm
Crigler-Najjar Syndrome - General Practice Notebook criglernajjar syndrome. crigler-najjar syndrome is a rare form of congenital non-haemolytic hyperbilirubinaemia. Type I Crigler-Najjar http://www.gpnotebook.co.uk/cache/349175813.htm
Extractions: Crigler-Najjar syndrome Crigler-Najjar syndrome is a rare form of congenital non-haemolytic hyperbilirubinaemia. Type I Crigler-Najjar syndrome is characterised by a total deficiency of hepatic glucuronyl transferase. It is inherited as an autosomal recessive. Conjugated bilirubin is absent from the serum. The majority die with kernicterus in the first year of life. Phototherapy can reduce the serum bilirubin by 50% and may be performed at home. Type II Crigler-Najjar syndrome is characterised by a partial deficiency of glucuronyl transferase. It is inherited as an autosomal dominant. Patients given phenobarbital often survive into adult life. Phototherapy may be used to lower the serum bilirubin level.
Crigler-Najjar Syndrome - General Practice Notebook criglernajjar syndrome. Medical search. crigler-najjar syndrome is a rare form of congenital non-haemolytic hyperbilirubinaemia. http://www.gpnotebook.co.uk/medwebpage.cfm?ID=349175813
Conditions And Diseases - Crigler-Najjar Syndrome Top Links criglernajjar syndrome Web Site Links. Austin Health Information - An overview of crigler-najjar syndrome including symptoms, treatment and prevention. http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
Crigler-Najjar Syndrome- Medcohealth.com criglernajjar syndrome. Source ADAM, Inc. Genetic counseling is recommended for prospective parents with a family history of crigler-najjar syndrome. http://www.medcohealth.com/medco/consumer/ehealth/ehsarticle.jsp?topicID=HE:Dise
Extractions: Crigler-Najjar Syndrome is a nearly always fatal genetic disorder that afflicts newborns. The disease is a deficiency in an enzyme that people need to control the production of bilirubin. When too much bilirubin accumulates, jaundice and severe brain damage occurs. Bilirubin is produced during the breakdown of hemoglobin, the blood's oxygen-carrying red pigment. Currently the disease is treated with phototherapy, to breakdown the bilirubin, followed by liver transplantation. However, liver transplantations may take place after permanent brain damage occurs. Investigators at The Rockefeller University have developed tin-mesoporphyrin, a drug that inhibits hemoglobin from breaking down. Currently, scientists are testing the drug in clinical trials. While the disease occurs worldwide, populations such as the Amish and Mennonites in which family and genetic histories can be established, afford an excellent opportunity for scientists and health care professionals to learn more about Crigler-Najjar Syndrome. Expected as attendees are a 31-year-old woman who is the oldest known living patient with Crigler-Najjar Syndrome, five Mennonite children with the disorder and their families as well as parents of patients from the United States, Canada, England, Germany and India.
Genetic Disorders: Crigler-Najjar Syndrome Genetic Disorders criglernajjar syndrome. An overview of crigler-najjar syndrome including symptoms, treatment and prevention. Crigler-Najjar Disease. http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Cr
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Crigler-Najjar Syndrome The New Health Directory, Directory, Home Health Conditions and Diseases Genetic Disorders criglernajjar syndrome (5) See Also http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/Cr
