scholarly journals Hereditary dysfunction of the third component of complement associated with a systemic lupus erythematosus-like syndrome and meningococcal meningitis

1992 ◽  
Vol 35 (5) ◽  
pp. 580-586 ◽  
Author(s):  
Ulf R. Nilsson ◽  
Bo Nilsson ◽  
Karl-Erik Storm ◽  
Gunilla Sjölin-Forsberg ◽  
Roger Hällgren
1981 ◽  
Vol 24 (10) ◽  
pp. 1255-1260 ◽  
Author(s):  
Yuji Sano ◽  
Hiroaki Nishimukai ◽  
Hajime Kitamura ◽  
Kazuyoshi Nagaki ◽  
Shinya Inai ◽  
...  

1977 ◽  
Vol 20 (7) ◽  
pp. 1304-1313 ◽  
Author(s):  
Lawrence D. Petz ◽  
Runas Powers ◽  
James R. Fries ◽  
Neil R. Cooper ◽  
Halsted R. Holman

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Marta Baleva ◽  
Krasimir Nikolov ◽  
Emil Manov ◽  
Anastas Stoikov ◽  
Rebhat Shabani ◽  
...  

We report four female patients with Graves' disease with positive ANA antibodies and possibility for development of systemic lupus erythematosus. All four patients have been treated with antithyroid drugs. SLE symptoms have appeared from 4 to 12 months after the beginning of therapy with methysol in two of them. The third patient had no symptoms for SLE, but her ANA, anti-DNA, and antihistone antibodies had been positive at the time of the onset of thyrotoxicosis. The fourth patient had alopecia areata with positive ANA and antihistone antibodies.


Lupus ◽  
2019 ◽  
Vol 28 (10) ◽  
pp. 1205-1213 ◽  
Author(s):  
E Z Zusman ◽  
E C Sayre ◽  
J A Aviña-Zubieta ◽  
M A De Vera

Objectives This study aimed to characterize the patterns of medication use before, during and after pregnancy in a population-based cohort of women with systemic lupus erythematosus (SLE). Methods Using population-based administrative data in British Columbia, Canada, with valid information on start date of pregnancy, we identified women with SLE who had singleton pregnancies ending in deliveries between January 1, 2002, and December 31, 2012. We assessed the proportion of SLE pregnancies exposed to SLE medications – namely antimalarials and immunosuppressants – as well as glucocorticosteroids, and nonsteroidal anti-inflammatory drugs (NSAIDs) 24 months before pregnancy, each trimester of pregnancy, and 12 months postpregnancy. We also assessed discontinuation of antimalarials and immunosuppressants, defined as no prescriptions in a given window following a prescription in a preceding window. Results Of 376 pregnancies (284 women) with SLE, 24.2% had one or more dispensing for antimalarials, 8.2% for azathioprine, 19.7% for glucocorticosteroids and 4.8% for NSAIDs during pregnancy. We observed a 16.7% discontinuation of antimalarials in the year prior to pregnancy, 29.8% in the first trimester, 9.7% in the second trimester, and 26.0% in the third trimester. We also observed a 29.2% discontinuation of azathioprine in the first trimester, 8.0% in the second trimester, and 9.1% in the third trimester. Conclusions These population-based data show frequent discontinuation of medications, particularly antimalarials, in SLE pregnancies. These findings suggest the importance of educating women with SLE who are pregnant or planning to become pregnant on the benefits and risks of medications during pregnancy.


PEDIATRICS ◽  
1964 ◽  
Vol 33 (3) ◽  
pp. 425-430
Author(s):  
Robert Jackson

This is the third reported case of discoid lupus erythematosus in a newborn infant, the first reported with a positive L.E. cell test in the infant's blood. The mother had systemic lupus erythematosus. The two previously reported cases and the nine previously reported cases of circulating L.E. cells in newborn infants whose mothers had systemic lupus erythematosus were reviewed. The tentative conclusion is reached that the presence of L.E. cells in the newborn circulation with or without accompanying discoid facial lupus erythematosus is due to the passive placental transfer of the L.E. factor from the mother to the fetus.


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