eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | lipoid proteinosis |
| Comorbidity | C0023795|lipoid proteinosis |
| Sentences | 2 |
| PubMedID- 22218285 | Methods: to investigate the brain's functional compensation of selective bilateral amygdala damage, we performed a series of behavioral, psychophysiological, and functional magnetic resonance imaging experiments in two adult female monozygotic twins (patient 1 and patient 2) with equivalent, extensive bilateral amygdala pathology as a sequela of lipoid proteinosis due to urbach-wiethe disease. |
| PubMedID- 22882737 | Neovascularization, pathologic, herpesvirus 8, macular degeneration, pathologic-von hippel–lindau disease, lymphangioleiomyomatosis, renal cell carcinoma, hereditary hemorrhagic telangiectasia, hemangioendothelioma, poems syndrome, essential osteolysis, capillary hemangioma kaposi sarcoma, rare diseases and lipoid proteinosis of urbach and wiethe) match with those pmids that are linked to mesh terms related to angiogenesis (angiogenesis inhibitors, vascular endothelial growth factor a, thalidomide, vascular endothelial growth factors, angiogenic proteins, vascular endothelial growth factor receptors). |
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