家族性非抱合型高ビリルビン血症
WordNet
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
- abnormally high amounts of bile pigment (bilirubin) in the blood
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
UpToDate Contents
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English Journal
- Italian guidelines for the management and treatment of neonatal cholestasis.
- Dani C1, Pratesi S2, Raimondi F3, Romagnoli C4; Task Force for Hyperbilirubinemia of the Italian Society of Neonatology.
- Italian journal of pediatrics.Ital J Pediatr.2015 Oct 1;41:69. doi: 10.1186/s13052-015-0178-7.
- Hyperbilirubinemia is a frequent condition affecting newborns during the first two weeks of life and when it lasts more than 14 days it is defined as prolonged jaundice. This condition requires differential diagnosis between the usually benign unconjugated hyperbilirubinemia and the pathological con
- PMID 26428285
- Human neonatal hepatocyte transplantation induces long-term rescue of unconjugated hyperbilirubinemia in the Gunn rat.
- Tolosa L1, López S1, Pareja E2, Donato MT1,3,4, Myara A5, Nguyen TH6, Castell JV1,3,4, Gómez-Lechón MJ1,3.
- Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.Liver Transpl.2015 Jun;21(6):801-11. doi: 10.1002/lt.24121.
- Crigler-Najjar type 1 disease is a rare inherited metabolic disease characterized by high levels of unconjugated bilirubin due to the complete absence of hepatic uridine diphosphoglucuronate-glucuronosyltransferase activity. Hepatocyte transplantation (HT) has been proposed as an alternative treatme
- PMID 25821167
- Unbound unconjugated hyperbilirubinemia is associated with central apnea in premature infants.
- Amin SB1, Wang H2.
- The Journal of pediatrics.J Pediatr.2015 Mar;166(3):571-5. doi: 10.1016/j.jpeds.2014.12.003. Epub 2015 Jan 14.
- OBJECTIVE: To evaluate whether jaundice, indexed by unbound bilirubin (UB), is associated with central apnea in premature infants.STUDY DESIGN: A prospective observational study was performed with 27-33 weeks' gestational age infants who were not requiring either mechanical ventilation or noninvasiv
- PMID 25596965
Japanese Journal
- 間接型高ビリルビン血症の分類と発生機序に関する考察:Crigler-Najjar症候群の一症例を中心とした検討
- 本邦における体質性黄疸の臨床統計:1970年より1974年までの全国調査から
Related Links
- 1. Semin Liver Dis. 1983 Feb;3(1):24-35. Familial unconjugated hyperbilirubinemia syndromes. Reichen J. Our understanding of the biochemical defects underlying the hepatic forms of congenital, unconjugated ...
- Familial unconjugated hyperbilirubinemia symptoms, causes, diagnosis, and treatment information for Familial unconjugated hyperbilirubinemia (Gilbert's Syndrome) with alternative diagnoses, full-text book chapters, misdiagnosis ... ...
★リンクテーブル★
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- 英
- familial unconjugated hyperbilirubinemia
- 同
- ルーシー・ドリスコール症候群 Lucey-Driscoll syndrome
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- 関
- family、family member、household、kindred
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- 関
- nonconjugated
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高非抱合型ビリルビン血症
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高ビリルビン血症