Bile duct paucity is part of the neonatal ichthyosis-sclerosing cholangitis phenotype

British Journal of Dermatology

Volumn 163, Issue 1, 2010, Pages 205-207

  Nagtzaam, I F ^a,b   Van Geel, M ^a,b   Driessen, A ^a   Steijlen, P M ^a,b   Van Steensel, M A M ^a,b  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^b MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

bile duct; claudin; ichthyosis; ichthyosis cholangitis; tight junction

Indexed keywords

ALPHA TOCOPHEROL; ARACHIS OIL; CLDN1 PROTEIN; DINUCLEOTIDE; PHENOBARBITAL; PROTEIN; RETINOL; UNCLASSIFIED DRUG; URSODEOXYCHOLIC ACID; VITAMIN D; VITAMIN K GROUP;

APGAR SCORE; ARTICLE; BILE DUCT DISEASE; BILE DUCT FIBROSIS; BILE DUCT HYPOPLASIA; BILE DUCT PAUCITY; BILIARY TRACT DISEASE; BIRTH WEIGHT; CASE REPORT; CHOLANGIOGRAPHY; CHOLESTASIS; CLINICAL FEATURE; CONTRACTURE; GENE; GENE DELETION; GENE MUTATION; HEPATITIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERBILIRUBINEMIA; HYPOTRICHOSIS; LAMELLAR ICHTHYOSIS; LIVER BIOPSY; LIVER FAILURE; LIVER TRANSPLANTATION; MALE; MOROCCO; NEONATAL ICHTHYOSIS SCLEROSING CHOLANGITIS; NEWBORN DISEASE; PARENT; PHENOTYPE; PHYSIOTHERAPY; POPULATION; PRIORITY JOURNAL; SCLEROSING CHOLANGITIS; SKIN; SKIN DEFECT;

BILE DUCTS; CHILD; CHOLANGITIS, SCLEROSING; CONSANGUINITY; DISEASE PROGRESSION; HOMOZYGOTE; HUMANS; ICHTHYOSIS; MALE; MUTATION; PEDIGREE; PHENOTYPE; SEQUENCE DELETION; TIGHT JUNCTIONS;

EID: 77954008878     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2010.09794.x     Document Type: Article

References (5)

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