Abstract
Carney Complex is a multiple endocrine neoplasia syndrome caused by a mutation in PRKAR1A gene. Tumor sites include skin (lentigines, blue nevus, cutaneous myxomas, palpebral lentigines), pituitary (somatotroph hyperplasia/adenomas), adrenal (primary pigmented nodular adrenal hyperplasia (PPNAD)), cardiac (myxomas), and testes (large cell calcifying sertoli cell tumor).We will present a family with a variety of distinct conditions related to Carney Complex, who were effectively treated to prevent secondary endocrine complications.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
