Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome
Pediatr Int
.
2007 Aug;49(4):540-2.
doi: 10.1111/j.1442-200X.2007.02410.x.
Authors
Kenichi Sugita
1
,
Yoshihiro Maruo
,
Hidemitsu Kurosawa
,
Akira Tsuchioka
,
Toshio Fujiwara
,
Asami Mori
,
Hiroshi Ideguchi
,
Mitsuoki Eguchi
Affiliation
1
Department of Pediatrics, Dokkyo University School of Medicine, Mibu, Tochigi, Japan. fwiw4736@mb.infoweb.ne.jp
PMID:
17587286
DOI:
10.1111/j.1442-200X.2007.02410.x
No abstract available
Publication types
Case Reports
MeSH terms
Child
Female
Gilbert Disease / complications*
Gilbert Disease / genetics
Glucuronosyltransferase / genetics
Humans
Hyperbilirubinemia / complications*
Mutation
Spherocytosis, Hereditary / complications*
Substances
Glucuronosyltransferase