PedAM
Pediatric Disease Annotations & Medicines
| Disease | nephrotic syndrome |
| Symptom | C1839611|n syndrome |
| Sentences | 4 |
| 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. |
| PubMedID- 24032283 | A novel mutation of laminin beta-2 gene in pierson syndrome manifested with nephrotic syndrome in the early neonatal period. |
| PubMedID- 25912097 | Underlying diseases treated by steroid administration were categorized as follows: systemic lupus erythematosus (sle), rheumatoid arthritis (ra), polymyositis/dermatomyositis, mixed connective tissue disease, sjögren syndrome, other types of collagen disease, nephrotic syndrome, nephritis, renal transplantation, other organ transplantation (except renal transplantation and bone marrow transplantation), hematological malignancy, thrombocytopenic purpura, aplastic anemia, inflammatory bowel disease, hepatitis, bronchial asthma, pulmonary disease (except asthma), skin disease, eye disease, ear disease, facial palsy, and other disease. |
| PubMedID- 22934182 | Β2-laminin deficiency in humans leads to familial nephrotic syndrome with ocular abnormalities—pierson syndrome . |
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