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1,347 Possible Causes for Gilbert Syndrome

  • Hereditary Spherocytosis

    We recently encountered a case of hereditary spherocytosis coexisting with Gilbert's syndrome.[ncbi.nlm.nih.gov] We experienced a case of a 19-year-old man with Gilbert syndrome with concomitant hereditary spherocytosis.[ncbi.nlm.nih.gov] We present a 17-year-old boy with hereditary spherocytosis coexisting with Gilbert's syndrome.[ncbi.nlm.nih.gov]

  • Transient Familial Neonatal Hyperbilirubinemia

    Genetics [ edit ] 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[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.[ipfs.io] 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]

  • 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] Kaplan M, Renbaum P Levi-Lahad A et al (1997) Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia[link.springer.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]

  • Progressive Familial Intrahepatic Cholestasis

    Progressive familial intrahepatic cholestasis (PFIC) is a group of inherited cholestatic conditions that develop as a result of impaired bile secretion. It manifests in infancy or childhood and can progress to failure to thrive or even advanced liver disease. Severe cases often require liver transplantation. The common[…][symptoma.com]

  • Fitzsimmons-McLachlan-Gilbert Syndrome

    Prevention - Fitzsimmons-McLachlan-Gilbert syndrome Not supplied. Diagnosis - Fitzsimmons-McLachlan-Gilbert syndrome Not supplied.[checkorphan.org] ORPHA:2824 Synonym(s): Fitzsimmons-McLachlan-Gilbert syndrome Prevalence: Inheritance: X-linked recessive Age of onset: Infancy ICD-10: G82.1 OMIM: 309560 UMLS: C2745996 MeSH[orpha.net] Syndrome “Fitzsimmons-Mclachlan-Gilbert Syndrome” In our body, the dis-order, Fitzsimmons-Mclachlan-Gilbert syndrome is a mental retardation with hereditary spastic paraplegia[wellnessadvocate.com]

  • Neonatal Jaundice

    The authors discuss the mechanism by which Gilbert's syndrome results in hyperbilirubinaemia and its similarities with Crigler-Najjar syndrome.[ncbi.nlm.nih.gov] The aim of this study was to detect the relationship between Gilbert's syndrome and hyperbilirubinemia in Gloucose-6-Phosphate Dehydrogenase (G6PD) deficient neonates.[ncbi.nlm.nih.gov] @article{Zahedpasha2014RelationBN, title {Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects.}, author {Yadollah[semanticscholar.org]

  • Jaundice

    Gilbert's syndrome requires no treatment.[mayoclinic.org] Gilbert Syndrome Gilbert syndrome is a common, harmless liver condition. It is a hereditary disorder affecting approximately 5-percent of the U. S. population.[activebeat.co] In most cases, two abnormal copies are needed to cause Gilbert's syndrome.[mayoclinic.org]

  • Gilbert Syndrome

    […] evidence of Gilbert's syndrome [ 11 ] .[patient.info] In certain cases, a genetic test may be necessary to confirm a diagnosis of Gilbert's syndrome. Living with Gilbert's syndrome Gilbert's syndrome is a lifelong disorder.[nhs.uk] […] jaundice Gilbert disease Gilbert-Lereboullet syndrome Gilbert's disease Gilbert's syndrome hyperbilirubinemia 1 Meulengracht syndrome unconjugated benign bilirubinemia Bosma[web.archive.org]

  • Crigler-Najjar Syndrome Type 1

    Heterozygotes of nonsense mutations (Q331X and C280X) in our previous study had either Crigler-Najjar syndrome type II or Gilbert's syndrome, but heterozygotes of R341X (mother[ncbi.nlm.nih.gov] BACKGROUND AND AIMS: Hereditary unconjugated hyperbilirubinemias, Crigler-Najjar syndrome type I, Crigler-Najjar syndrome type II (CN-2), and Gilbert syndrome (GS) all result[ncbi.nlm.nih.gov] Heirwegh Bilirubin pigments were studied in the bile of 20 normal adults, 25 patients with Gilbert's syndrome, 9 children with Crigler-Najjar disease, and 6 patients with[jci.org]

  • Rotor Syndrome

    Inherited non-haemolytichyperbilirubinemic conditions include Dubin-Johnson, Rotor, and Gilbert-Meulengracht syndromes, which are important differential diagnoses indicating[ncbi.nlm.nih.gov] Here are a few syndromes that are easy to mix up: Crigler-Najjar, Gilbert, Dubin-Johnson, and Rotor syndromes.[pathologystudent.com] From these results, the case was diagnosed as Gilbert’s syndrome combined with macroamylasemia.[link.springer.com]

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