ISSN:
2213-8595
Content:
Multiple endocrine neoplasia type 2B is a rare syndrome caused mainly by Met918Thr germline RET mutation, and characterised by medullary thyroid carcinoma, phaeochromocytoma, and extra-endocrine features. Data are scarce on the natural history of multiple endocrine neoplasia type 2B. We aimed to advance understanding of the phenotype and natural history of multiple endocrine neoplasia type 2B, to increase awareness and improve detection.
In:
The lancet. Diabetes & Endocrinology, Oxford : Elsevier, 2013, 7(2019), 3, Seite 213-220, 2213-8595
In:
volume:7
In:
year:2019
In:
number:3
In:
pages:213-220
Language:
English
DOI:
10.1016/S2213-8587(18)30336-X
Author information:
Bausch, Birke 1977-
Author information:
Korbonits, Márta
Author information:
Dralle, Henning 1950-
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