Disease | c syndrome |
Phenotype | C0030421|paraganglioma |
Sentences | 3 |
PubMedID- 20514823 | A diagnosis of phaeochromocytoma is suspected by typical paroxysmal symptoms, unusual or refractory hypertension, discovery of an adrenal incidentaloma or a family history of phaeochromocytoma or paraganglioma, possibly associated with other genetic syndromes (multiple endocrine neoplasia type 2 a or b, neurofibromatosis type 1 and von hippel-lindau disease). |
PubMedID- 22446654 | The clinical and laboratory study of classic syndromes associated with paraganglioma was negative. |
PubMedID- 22987597 | Hypopharyngeal paraganglioma with a paraneoplastic neurologic syndrome: a case report. |
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