eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | nephrotic syndrome |
| Symptom | C1839611|n syndrome |
| Sentences | 3 |
| PubMedID- 24032283 | A novel mutation of laminin beta-2 gene in pierson syndrome manifested with nephrotic syndrome in the early neonatal period. |
| PubMedID- 22934182 | Β2-laminin deficiency in humans leads to familial nephrotic syndrome with ocular abnormalities—pierson syndrome . |
| PubMedID- 20224959 | Some % totals do not equal 100% owing to rounding; *there was no available information regarding gender for five patients and age at diagnosis for 60 patients.table 5underlying illness for which patients with steroid-induced onfh received steroid therapyunderlying illnessnumber (%)systemic lupus erythematosus236 (31.2)rheumatoid arthritis7 (0.9)polymyositis/dermatomyositis37 (4.9)mixed connective tissue disease20 (2.6)sjöegren syndrome8 (1.1)other type of collagen disease21 (2.8)nephrotic syndrome48 (6.3)nephritis19 (2.5)renal transplantation27 (3.6)other organ transplantation10 (1.3)thrombocytopenic purpura33 (4.4)aplastic anemia13 (1.7)hepatitis6 (0.8)bronchial asthma34 (4.5)pulseless disease1 (0.1)skin disease19 (2.5)eye disease32 (4.2)other disease186 (24.6)onfh, osteonecrosis of the femoral head; analysis is based on 760 subjects with history of systemic steroid administration. |
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