In:
Hepatology, Ovid Technologies (Wolters Kluwer Health), Vol. 66, No. 1 ( 2017-07), p. 286-288
Kurzfassung:
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).
Materialart:
Online-Ressource
ISSN:
0270-9139
,
1527-3350
Sprache:
Englisch
Verlag:
Ovid Technologies (Wolters Kluwer Health)
Publikationsdatum:
2017
ZDB Id:
1472120-X
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