Multiple endocrine neoplasia type II
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Multiple endocrine neoplasia type II (MEN2) is also known as mucosal neuroma syndrome or multiple endocrine adenomatosis. It is a collection of syndromes characterised by the presence of multiple endocrine tumours.
They are autosomal dominant in inheritance, and share medullary thyroid carcinoma as a feature. They are divided into:
-
MEN2a
or Sipple(Sipple syndrome) - MEN2b (mucosal neuroma syndrome)
- familial medullary thyroid carcinoma
See also
-
MEN1
orWermer(Wermer syndrome) -
MEN2 (multiple endocrine adenomatosis)
- MEN2a (Sipple syndrome)
- MEN2b (mucosal neuroma syndrome)
- familial medullary thyroid carcinoma
- MEN4
- Carney complex
-<a href="/articles/multiple-endocrine-neoplasia-type-iia-1">MEN2a</a> or Sipple syndrome</li>-<li><a href="/articles/multiple-endocrine-neoplasia-type-iib">MEN2b</a></li>- +<a href="/articles/multiple-endocrine-neoplasia-type-iia-1">MEN2a</a> (Sipple syndrome)</li>
- +<li>
- +<a href="/articles/multiple-endocrine-neoplasia-type-iib">MEN2b</a> (mucosal neuroma syndrome)</li>
- +<li><a href="/articles/familial-medullary-thyroid-carcinoma">familial medullary thyroid carcinoma</a></li>
- +</ul><h4>See also</h4><ul>
- +<li>
- +<a href="/articles/multiple-endocrine-neoplasia-type-i-1">MEN1</a> (Wermer syndrome)</li>
- +<li>
- +<strong>MEN2 (multiple endocrine adenomatosis)</strong><ul>
- +<li>
- +<a href="/articles/multiple-endocrine-neoplasia-type-iia-1">MEN2a</a> (Sipple syndrome)</li>
- +<li>
- +<a href="/articles/multiple-endocrine-neoplasia-type-iib">MEN2b</a> (mucosal neuroma syndrome)</li>
-</ul><h4>See also</h4><ul><li>-<a href="/articles/men_i">MEN1</a> or <a href="/articles/wermer-syndrome">Wermer syndrome</a>-</li></ul>- +</ul>
- +</li>
- +<li><a href="/articles/multiple-endocrine-neoplasia-type-iv">MEN4</a></li>
- +<li><a href="/articles/carney-complex">Carney complex</a></li>
- +</ul>
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