A case of multiple endocrine neoplasia type 2B undiagnosed for many years despite its typical phenotype

Endocrine

Volumn 15, Issue 2, 2001, Pages 143-146

  Ohyama, Tomoyo ^a   Sato, Makoto ^a   Murao, Koji ^a   Kittaka, Katsuji ^a   Namihira, Hiroyoshi ^a   Matsubara, Shuji ^a   Imachi, Hitomi ^a   Yamauchi, Kiyoaki ^a   Takahara, Jiro ^a  

^a KAGAWA UNIVERSITY   (Japan)

Author keywords

Ganglioneuromatosis; Medullary thyroid carcinoma; Multiple endocrine neoplasia type 2B; Mutation; Pheochromocytoma

Indexed keywords

ADRENAL MEDULLA TUMOR; ADULT; ARTICLE; CASE REPORT; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; FEMALE; GANGLIONEUROMA; GOITER; HUMAN; NEUROFIBROMATOSIS; PHENOTYPE; PHEOCHROMOCYTOMA; POINT MUTATION; PRIORITY JOURNAL; THYROID CARCINOMA;

EID: 0034776719     PISSN: 1355008X     EISSN: None     Source Type: Journal    
DOI: 10.1385/ENDO:15:2:143     Document Type: Article

References (6)