eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pierson syndrome |
| Comorbidity | C0027726|nephrotic syndrome |
| Sentences | 2 |
| PubMedID- 22934182 | Β2-laminin deficiency in humans leads to familial nephrotic syndrome with ocular abnormalities—pierson syndrome [45]. |
| PubMedID- 24032283 | A novel mutation of laminin beta-2 gene in pierson syndrome manifested with nephrotic syndrome in the early neonatal period. |
Page: 1