scholarly journals Pulmonary renal syndrome in a child with coexistence of anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane disease: case report and literature review

2013 ◽  
Vol 14 (1) ◽  
Author(s):  
Radovan Bogdanović ◽  
Predrag Minić ◽  
Jasmina Marković-Lipkovski ◽  
Nataša Stajić ◽  
Nataša Savić ◽  
...  
2021 ◽  
Vol 69 (4) ◽  
pp. 103304
Author(s):  
Rafael Hernani ◽  
Asunción Sancho ◽  
Paula Amat ◽  
Juan Carlos Hernández-Boluda ◽  
Ariadna Pérez ◽  
...  

Pharmacology ◽  
2011 ◽  
Vol 87 (5-6) ◽  
pp. 318-320 ◽  
Author(s):  
Aymen Zayen ◽  
Henda Rais ◽  
Hela Rifi ◽  
Mouna Ouarda ◽  
Mehdi Afrit ◽  
...  

2021 ◽  
Vol 78 ◽  
pp. 151-154
Author(s):  
Kaoutar Chaker ◽  
Omar Berrada ◽  
Mouna Lyoubi ◽  
Youssef Oukessou ◽  
Reda Allah Abada ◽  
...  

2015 ◽  
Vol 84 (3) ◽  
pp. 201-204
Author(s):  
Jakub Żurawski

Initially, the thin glomerular basement membrane disease was called “a gentle and curable hemorrhagic nephritis”. The thin basement membrane disease has been finally characterized at the beginning of 1970s. This is when the connection between previously clinically described gentle microhematuria and significant thinning of glomerular basement membrane discovered during examination under the electron-microscope has been established. Ultimately, the disease has been described as a condition characterized with a diverse clinical course, usually mild, but sometimes progressive. It is a family conditioned disease, but it also appears sporadically and concerns at least 1% of the population. It has also been stated that it is one of the most frequent renal diseases, enumerated directly after changes caused by infections, hypertension and renal lithiasis. This particular disease is diagnosed more often than IgA nephropathy and Alport syndrome, which are also associated with haematuria or microhematuria.


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