Abstract
We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 29-38 |
| Number of pages | 10 |
| Journal | Journal of Radiology Case Reports |
| Volume | 6 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 1 2012 |
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Keywords
- Alagille syndrome
- Biliary ducts
- Cholestasis
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging
Cite this
Paucity of biliary ducts : A rare etiology of neonatal cholestasis. / Figiel, Steven Cornell; Franco, Arie; Pucar, Darko; Lewis, Kristopher Neal; Lee, Jeffrey Roberts.
In: Journal of Radiology Case Reports, Vol. 6, No. 2, 01.02.2012, p. 29-38.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Paucity of biliary ducts
T2 - A rare etiology of neonatal cholestasis
AU - Figiel, Steven Cornell
AU - Franco, Arie
AU - Pucar, Darko
AU - Lewis, Kristopher Neal
AU - Lee, Jeffrey Roberts
PY - 2012/2/1
Y1 - 2012/2/1
N2 - We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.
AB - We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and radiologic findings. We also discuss the various etiologies of cholestasis that are included in the differential diagnosis.
KW - Alagille syndrome
KW - Biliary ducts
KW - Cholestasis
UR - http://www.scopus.com/inward/record.url?scp=84863142456&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84863142456&partnerID=8YFLogxK
U2 - 10.3941/jrcr.v6i2.892
DO - 10.3941/jrcr.v6i2.892
M3 - Article
C2 - 22690284
AN - SCOPUS:84863142456
VL - 6
SP - 29
EP - 38
JO - Journal of Radiology Case Reports
JF - Journal of Radiology Case Reports
SN - 1943-0922
IS - 2
ER -