A case report: Alagille syndrome

Alagille syndrome consists of 5 major features comprising paucity of interlobular bile ducts, characteristic facies, posterior embryotoxon, vertebral defects and peripheral pulmonic stenosis. The female patient in this report met 4 of the 5 major features except ocular abnormality. The first clinica...

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Main Authors:	Ukarapol N., Wongsawasdi L., Sittiwangkul R.
Format:	Case Reports
Language:	English
Published:	2014
Online Access:	http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3317
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Institution:	Chiang Mai University
Language:	English

id	th-cmuir.6653943832-3317
record_format	dspace
spelling	th-cmuir.6653943832-33172014-08-30T02:26:00Z A case report: Alagille syndrome Ukarapol N. Wongsawasdi L. Sittiwangkul R. Alagille syndrome consists of 5 major features comprising paucity of interlobular bile ducts, characteristic facies, posterior embryotoxon, vertebral defects and peripheral pulmonic stenosis. The female patient in this report met 4 of the 5 major features except ocular abnormality. The first clinical presentations were prolonged jaundice and generalized ecchymoses. She was treated by plasma replacement and vitamin supplement, particularly vitamin K1, which produced clinical improvement. This report also reviews the literature of Alagille syndrome. 2014-08-30T02:26:00Z 2014-08-30T02:26:00Z 2000 Case Reports 0125-2208 10808707 http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3317 eng
institution	Chiang Mai University
building	Chiang Mai University Library
country	Thailand
collection	CMU Intellectual Repository
language	English
description	Alagille syndrome consists of 5 major features comprising paucity of interlobular bile ducts, characteristic facies, posterior embryotoxon, vertebral defects and peripheral pulmonic stenosis. The female patient in this report met 4 of the 5 major features except ocular abnormality. The first clinical presentations were prolonged jaundice and generalized ecchymoses. She was treated by plasma replacement and vitamin supplement, particularly vitamin K1, which produced clinical improvement. This report also reviews the literature of Alagille syndrome.
format	Case Reports
author	Ukarapol N. Wongsawasdi L. Sittiwangkul R.
spellingShingle	Ukarapol N. Wongsawasdi L. Sittiwangkul R. A case report: Alagille syndrome
author_facet	Ukarapol N. Wongsawasdi L. Sittiwangkul R.
author_sort	Ukarapol N.
title	A case report: Alagille syndrome
title_short	A case report: Alagille syndrome
title_full	A case report: Alagille syndrome
title_fullStr	A case report: Alagille syndrome
title_full_unstemmed	A case report: Alagille syndrome
title_sort	case report: alagille syndrome
publishDate	2014
url	http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3317
_version_	1681420025500532736

A case report: Alagille syndrome

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