eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | sturge weber syndrome |
| Comorbidity | C0235752|port-wine stain |
| Sentences | 6 |
| PubMedID- 21906147 | sturge-weber syndrome in patients with facial port-wine stain. |
| PubMedID- 25657402 | Hereby, we report a case where our patient presented with port-wine stain, nevus of ota, sturge-weber syndrome, and klippel-trenaunay syndrome; which has made it a rare combination. |
| PubMedID- 25592619 | A prospective study of risk for sturge-weber syndrome in children with upper facial port-wine stain. |
| PubMedID- 22132016 | port-wine stain of sturge-weber syndrome and café- au- lait pigmentation of neurofibromatosis are the major differential diagnoses for nevus of ota.1213 the various treatment modalities available for nevus of ota involving the skin includes dermabrasion, epidermal peeling and argon laser. |
| PubMedID- 24207015 | port-wine stains in patients with sturge-weber syndrome often distribute in the facial areas innervated by the first (v1) and second (v2) branches of trigeminal nerve, while the third (v3) branch and contralateral face can also be involved in some cases. |
| PubMedID- 26064732 | [11] reported a case with port-wine stain, nevus of ota, sturge-weber syndrome, and klippel-trénaunay syndrome. |
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