WordNet
- abnormally high amounts of bile pigment (bilirubin) in the blood
PrepTutorEJDIC
- 世襲の,親譲りの / 遺伝的な,遺伝性の
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/09/02 09:51:47」(JST)
wiki en
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 黄疸または無症候性高ビリルビン血症成人患者に対する診断的アプローチ diagnostic approach to the adult with jaundice or asymptomatic hyperbilirubinemia
- 2. 術後黄疸患者に対するアプローチ approach to the patient with postoperative jaundice
- 3. 小児における非抱合型高ビリルビン血症による黄疸の評価 evaluation of jaundice caused by unconjugated hyperbilirubinemia in children
- 4. ビリルビン過剰産生によるジルベール症候群および非抱合型ビリルビン過剰産生 gilbert syndrome and unconjugated hyperbilirubinemia due to bilirubin overproduction
- 5. 新生児における非抱合型高ビリルビン血症の発症機序および病因 pathogenesis and etiology of unconjugated hyperbilirubinemia in the newborn
English Journal
- A Pediatrician's Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in Neonates.
- Christensen RD1, Yaish HM2, Gallagher PG3.
- Pediatrics.Pediatrics.2015 Jun;135(6):1107-1114.
- Newborn infants who have hereditary spherocytosis (HS) can develop anemia and hyperbilirubinemia. Bilirubin-induced neurologic dysfunction is less likely in these neonates if the diagnosis of HS is recognized and appropriate treatment provided. Among neonates listed in the USA Kernicterus Registry,
- PMID 26009624
- Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.
- Christensen RD1, Agarwal AM2, Nussenzveig RH3, Heikal N2, Liew MA3, Yaish HM4.
- Journal of perinatology : official journal of the California Perinatal Association.J Perinatol.2015 May;35(5):357-61. doi: 10.1038/jp.2014.202. Epub 2014 Nov 6.
- OBJECTIVE: Neonates with undiagnosed hereditary spherocytosis (HS) are at risk for developing hazardous hyperbilirubinemia and anemia. Making an early diagnosis of HS in a neonate can prompt anticipatory guidance to prevent these adverse outcomes. A recent comparison study showed that a relatively n
- PMID 25357094
- [Hereditary spherocytosis. Review. Part II. Symptomatology, outcome, complications, and treatment].
- Comité Nacional de Hematología, Donato H, Crisp RL, Rapetti MC, García E, Attie M.
- Archivos argentinos de pediatría.Arch Argent Pediatr.2015 Apr;113(2):168-76. doi: 10.1590/S0325-00752015000200025.
- Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid
- PMID 25727830
Japanese Journal
- Hereditary Spherocytosis in a Middle-aged Man Complicated with Common Bile Duct Stones
- Internal Medicine 54(12), 1509-1512, 2015
- NAID 130005075955
- Eosin-5-maleimide を用いた赤血球膜 band 3 定量法により新生児期に診断しえた遺伝性球状赤血球症の2例
- 日本周産期・新生児医学会雑誌 = Journal of Japan Society of Perinatal and Neonatal Medicine 45(1), 166-170, 2009-04-25
- NAID 10025167909
- Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome
- Pediatrics international : official journal of the Japan Pediatric Society 49(4), 540-542, 2007-08-01
- NAID 10019815055
Related Links
- Hyperbilirubinemia, Hereditary; Rotor Syndrome. On-line free medical diagnosis assistant. Ranked list of possible diseases from either several symptoms or a full patient history. A similarity measure between symptoms and diseases ... ...
- RecentMedicalFindings (RMF) takes different health and medical topics, and searches millions of trust-worthy peer-reviewed biomedical articles, published in a wide collection of scientific journals. RMF then extracts the most ...
Related Pictures
★リンクテーブル★
| リンク元 | 「先天性ビリルビン代謝異常症」「遺伝性高ビリルビン血症」 |
| 関連記事 | 「hereditary」「hyperbilirubinemia」 |
「先天性ビリルビン代謝異常症」
- 英
- inborn error of bilirubin metabolism
- 同
- 先天性黄疸 congenital jaundice、体質性黄疸 constitutional jaundice、遺伝性高ビリルビン血症 hereditary hyperbilirubinemia
「遺伝性高ビリルビン血症」
「hereditary」
- adj.
- 遺伝性の、遺伝の