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PedAM

Pediatric Disease Annotations & Medicines




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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