310 A Case Report of Thin Basement Membrane with Proteinuria Associated with Complement 5 and Apolipoprotein L1 Variants in the Heterozygous State

2021 ◽  
Vol 77 (4) ◽  
pp. 664
PEDIATRICS ◽  
1965 ◽  
Vol 35 (6) ◽  
pp. 1008-1010
Author(s):  
A. F. ROBERTSON

A case is presented in which biliary atresia and the heterozygous state of galactosemia occurred coincidentally. The mother was also heterozygous for galactosemia. A liver biopsy revealed changes compatible with biliary atresia and no evidence of galactosemia cirrhosis.


2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Keiko Oda ◽  
Kan Katayama ◽  
Akiko Tanoue ◽  
Tomohiro Murata ◽  
Yumi Hirota ◽  
...  

2006 ◽  
Vol 10 (1) ◽  
pp. 55-58 ◽  
Author(s):  
Eduardo José Bellotto Monteiro ◽  
Daiane Caron ◽  
Carlos Alberto Balda ◽  
Marcello Franco ◽  
Aparecido Bernardo Pereira ◽  
...  

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