ルーシー・ドリスコール症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- United States playwright and public official (1902-1987) (同)Clare Booth Luce
- United States publisher of magazines (1898-1967) (同)Henry Luce, Henry Robinson Luce
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/06/18 23:59:33」(JST)
[Wiki en表示]
Lucey–Driscoll syndrome |
Classification and external resources |
ICD-9 |
774.30 |
OMIM |
237900 |
DiseasesDB |
32677 |
Lucey–Driscoll syndrome is an autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism. It is one of several disorders classified as a transient familial neonatal unconjugated hyperbilirubinemia.
Cause
The common cause is congenital, but it can also be caused by maternal steroids passed on through breast milk to the newborn. It is different from breast feeding-associated jaundice (breast-fed infants have higher bilirubin levels than formula-fed ones).
Genetics
Lucey–Driscoll syndrome has an autosomal recessive pattern of inheritance.
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.
External links
- Online 'Mendelian Inheritance in Man' (OMIM) 237900 - transient familial neonatal hyperbilirubinemia, breast feeding jaundice included
- Hyperbilirubinemia, Unconjugated at eMedicine
- Lucey Driscoll syndrome at NIH's Office of Rare Diseases
Heme metabolism disorders (E80, 277.1, 277.4)
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Porphyria,
hepatic and erythropoietic
(porphyrin) |
early mitochondrial: |
- ALAD porphyria
- Acute intermittent porphyria
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cytoplasmic: |
- Gunther disease/congenital erythropoietic porphyria
- Porphyria cutanea tarda/Hepatoerythropoietic porphyria
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late mitochondrial: |
- Hereditary coproporphyria
- Harderoporphyria
- Variegate porphyria
- Erythropoietic protoporphyria
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Hereditary hyperbilirubinemia
(bilirubin) |
unconjugated: |
- Gilbert's syndrome
- Crigler–Najjar syndrome
- Lucey–Driscoll syndrome
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conjugated: |
- Dubin–Johnson syndrome
- Rotor syndrome
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mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m
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k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon
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m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
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cell/phys (coag, heme, immu, gran), csfs
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rbmg/mogr/tumr/hist, sysi/epon, btst
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drug (B1/2/3+5+6), btst, trns
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UpToDate Contents
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English Journal
- [Lucey-Driscoll syndrome].
- Imai T1, Isobe K.
- Ryōikibetsu shōkōgun shirīzu.Ryoikibetsu Shokogun Shirizu.1995;(8):440-1.
- PMID 8581674
- [Lucey-Driscoll syndrome].
- Oda T.
- Nihon rinsho. Japanese journal of clinical medicine.Nihon Rinsho.1977 Spring;35 Suppl 1:1056-7.
- PMID 612731
Related Pictures
★リンクテーブル★
[★]
- 英
- Lucey-Driscoll syndrome
- 同
- Lucey-Driscoll症候群
- 関
- 家族性非抱合型高ビリルビン血症。間接ビリルビン、黄疸、母乳、UGT
[★]
- 英
- familial unconjugated hyperbilirubinemia
- 同
- ルーシー・ドリスコール症候群 Lucey-Driscoll syndrome
[★]