In:
Hepatology, Ovid Technologies (Wolters Kluwer Health), Vol. 66, No. 1 ( 2017-07), p. 286-288
Abstract:
A 52‐year old patient presented with lymphedema, protein loosing enteropathy, and sclerosing cholangitis and was diagnosed with lymphedema cholestasis syndrome (LCS). Cholangioscopy revealed dilated lymphatic vessels obstructing the bile duct and compound heterozygosity for collagen and calcium‐binding epidermal growth factor domain‐containing protein 1 ( CCBE1 ) mutations was identified defining a novel type of LCS. (H epatology 2017;66:286–288).
Type of Medium:
Online Resource
ISSN:
0270-9139
,
1527-3350
Language:
English
Publisher:
Ovid Technologies (Wolters Kluwer Health)
Publication Date:
2017
detail.hit.zdb_id:
1472120-X
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