SERUM ALPHA-FETOPROTEIN LEVELS IN EXTRAHEPATIC BILIARY ATRESIA, IDIOPATHIC NEONATAL HEPATITIS AND ALPHA-1-ANTITRYPSIN DEFICIENCY (PiZ)

1976 ◽  
Vol 65 (4) ◽  
pp. 623-629 ◽  
Author(s):  
D. I. JOHNSTON ◽  
A. P. MOWAT ◽  
HILARY ORR ◽  
J. KOHN
PEDIATRICS ◽  
1992 ◽  
Vol 89 (2) ◽  
pp. 329-330
Author(s):  
PIETRO VAJRO ◽  
ANGIOLA FONTANELLA ◽  
EMILIA VUTTARIELLO ◽  
ANNA DE VINCENZO ◽  
GIULIANA FORTUNATO

For the practicing pediatrician, the most commonly encountered causes of neonatal cholestasis are idiopathic neonatal hepatitis (INH) and extrahepatic biliary atresia (EHBA). However, despite extensive research, little improvement in our understanding of the etiology of INH and EHBA has occurred.1 It has been proposed that both of them may be part of a continuum of hepatobiliary disease caused by a common insult with a different predominant injury site.2 In this respect, it is interesting that, up to the present, several cases of discordance for EHBA in twins of various zygosity have been reported,3-8 whereas no data are available about either concordance or discordance for INH both in monozygotic and dizygotic twins.


The Lancet ◽  
1974 ◽  
Vol 303 (7854) ◽  
pp. 373-375 ◽  
Author(s):  
PaulM. Zeltzer ◽  
EricW. Fonkalsrud ◽  
RobertC. Neerhout ◽  
E.Richard Stiehm

The Lancet ◽  
1974 ◽  
Vol 304 (7881) ◽  
pp. 650-651 ◽  
Author(s):  
C.A. Kattamis ◽  
Sophia Laskari ◽  
N.S. Matsaniotis

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
Andrew W. Wang ◽  
Kimberly Newton ◽  
Karen Kling

We describe the rare instance of concomitant biliary atresia and alpha-1-antitrypsin deficiency and the first documented successful portoenterostomy in this scenario. The potential for dual pathology must be recognized and underscores that prompt diagnosis of biliary atresia, despite concomitant alpha-1-antitrypsin deficiency, is essential to afford potential longstanding native liver function.


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