eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | c syndrome |
| Comorbidity | C0031511|pheochromocytoma |
| Sentences | 4 |
| PubMedID- 24472290 | pheochromocytoma can be associated with certain genetic syndromes such as multiple endocrine neoplasia type 2 (men 2), neurofibromatosis (nf) and von hippel-lindau (vhl) syndrome. |
| PubMedID- 25136447 | Learning points: recurrent benign pheochromocytomas should raise suspicion of a genetic syndrome.a pheochromocytoma at a young age has a high propensity to recur and strict follow-up is mandatory. |
| PubMedID- 24981168 | We reported two cases of bilateral pheochromocytoma associated with men 2 syndrome cured by simultaneous bilateral laparoscopic adrenalectomy. |
| PubMedID- 22571874 | Numerous named genetic syndromes have been associated with pheochromocytoma and paraganglioma. |
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