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(→Pituitary adenoma: +syndrome, tweak, wikify) |
(→Familial pituitary adenomas: tweak) |
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| MEN-1-like syndrome | | MEN-1-like syndrome | ||
| CDKN1B<ref name=omim600778>{{OMIM|600778}}</ref> | | CDKN1B<ref name=omim600778>{{OMIM|600778}}</ref> | ||
| known as ''Multiple endocrine neoplasia IV''<ref name=omim600778>{{OMIM|600778}}</ref> | | also known as ''Multiple endocrine neoplasia IV'' <ref name=omim600778>{{OMIM|600778}}</ref> | ||
|- | |- | ||
| [[Carney syndrome]] | | [[Carney syndrome]] | ||
| PRKAR1A | | PRKAR1A | ||
| | | other findings (mnemonic ''NAME''): nevi, [[atrial myxoma]], myxoid neurofibroma, ephelides (freckles) | ||
|- | |- | ||
| | | Isolated pituitary adenoma<ref name=pmid22612670>{{Cite journal | last1 = Korbonits | first1 = M. | last2 = Storr | first2 = H. | last3 = Kumar | first3 = AV. | title = Familial pituitary adenomas - Who should be tested for AIP mutations? | journal = Clin Endocrinol (Oxf) | volume = | issue = | pages = | month = May | year = 2012 | doi = 10.1111/j.1365-2265.2012.04445.x | PMID = 22612670 }}</ref> | ||
| AIP | | AIP | ||
| classically GH-producing adenoma - | | classically GH-producing adenoma - leads to acromegaly | ||
|} | |} | ||
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