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695 Possible Causes for Crigler-Najjar Syndrome

  • Bilirubin Encephalopathy

    Abstract Children with Crigler-Najjar syndrome type I are at increased risk for neurologic deficits.[ncbi.nlm.nih.gov] The latter is seen in a rare defect of glucuronyl transferase, the Crigler-Najjar syndrome, and in premature babies in whom this enzyme is not fully functional.[neuropathology-web.org] Crigler-Najjar syndrome ) acquired defects in bilirubin conjugation (e.g.[radiopaedia.org]

  • Crigler-Najjar Syndrome

    There are no guidelines for prevention of Crigler-Najjar syndrome.[symptoma.com] CriglerNajjar syndrome and Gilbert syndrome In CriglerNajjar syndrome and Gilbert syndrome, routine liver function tests are normal, and hepatic histology usually is normal[en.wikipedia.org] Najjar syndrome Crigler-Najjar syndrome, type I (disorder) CriglerNajjar syndrome Crigler-Najjar syndrome, type I edit English Crigler-Najjar syndrome bilirubin metabolic[wikidata.org]

  • Hepatitis

    Sexual Transmission of Hepatitis C April 5, 2007 Printer-friendly version Important research examining the risks of Hepatitis C transmission through heterosexual relationships has recently been conducted. Discover whether heterosexual couples were found to be at an increased risk for acquiring HCV in consideration[…][web.archive.org]

  • Crigler-Najjar Syndrome Type 2

    Crigler-Najjar syndrome may be suspected in neonates if jaundice lasts longer than usual.[symptoma.com] Abstract Crigler-Najjar syndrome is a rare disorder of bilirubin metabolism with two distinct forms: type 1 and type 2.[ncbi.nlm.nih.gov] […] full list of Crigler-Najjar syndrome, type 2 signs or Crigler-Najjar syndrome, type 2 symptoms.[checkorphan.org]

  • Gilbert's Disease

    There are two forms: Crigler-Najjar syndrome type 1 (CN-1) and Crigler-Najjar syndrome type 2 (CN-2).[rarediseases.info.nih.gov] People with Gilbert syndrome have a normal life expectancy. [1] Of note, mutations in the UGT1A1 gene can alternatively cause other disorders, such as Crigler-Najjar syndrome[rarediseases.info.nih.gov]

  • Transient Familial Neonatal Hyperbilirubinemia

    A defect in the UGT1A1 -gene, also linked to CriglerNajjar syndrome and Gilbert's syndrome, is responsible for the congenital form of Lucey–Driscoll syndrome.[ipfs.io] Genetics [ edit ] A defect in the UGT1A1 -gene, also linked to CriglerNajjar syndrome and Gilbert's syndrome, is responsible for the congenital form of Lucey–Driscoll syndrome[en.wikipedia.org] A defect in the UGT1A1 -gene, also linked to Crigler-Najjar syndrome and Gilbert's syndrome, is responsible for the congenital form of Lucey-Driscoll syndrome.[wikidoc.org]

  • Rotor Syndrome

    syndrome.[ncbi.nlm.nih.gov] Crigler-Najjar syndrome There are actually two types of Crigler-Najjar, and boy are they different clinically.[pathologystudent.com] Crigler FJ, Najjar VA. Congenital familial nonhemolytic jaundice with kernicterus. Pediatrics. 1952;10:169-170. INTERNET Labrune P. Crigler-Najjar syndrome type 1.[rarediseases.org]

  • Physiological Neonatal Jaundice

    Phenobarbital (Gardenal) is an enzyme inducer which is generally given for other, more serious, causes of high bilirubin such as Crigler-Najjar Syndrome, Gilberts syndrome[doctor.ndtv.com] Possible conditions include hemolytic anemias, blood group incompatibilities, Gilbert and CriglerNajjar syndromes, glucose-6-phosphate dehydrogenase ( G6PD ) deficiency,[amboss.com] Dubin-Johnson sydrome; Gilbert’s syndrome; Crigler-Najjar syndrome Causes of prolonged jaundice include hypothyroidism/hypopituitarism; Breast milk jaundice; GI causes e.g[dundeemedstudentnotes.wordpress.com]

  • Labrune Syndrome

    […] a rare liver disease, Crigler-Najjar Syndrome. (12/02/2018)[genethon.fr] Crigler-Najjar syndrome type I Crigler-Najjar syndrome type II (Arias syndrome) General Discussion Summary Crigler-Najjar syndrome is a rare genetic disorder characterized[rarediseases.org] . / Current therapy for Crigler-Najjar syndrome type 1 : Report of a world registry .[rug.nl]

  • Dubin-Johnson Syndrome

    syndrome.[ncbi.nlm.nih.gov] Crigler-Najjar syndrome There are actually two types of Crigler-Najjar, and boy are they different clinically.[pathologystudent.com] Gilbert-Meulengracht disease leads to unconjugated hyperbilirubinemia because of impaired glucuronidation activity, and is part of a spectrum of genetic variants also encompassing fatal Crigler-Najjar[ncbi.nlm.nih.gov]

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