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ve text.Written by experts in the field.Includes supplementaThis book is designed to present a comprehensive and state-of the-art approach to the management of adrenal neoplasms that provides a resource to the broad group of providers that will encounter such a patient. Sections address issues thatInitial 发表于 2025-3-22 10:22:40
Genetics of Benign Adrenocortical Tumors,recently linked to . defects; the ARMC5 protein has an unknown function. Finally, benign ACTs are found in the context of a number of other conditions from multiple endocrine neoplasia type 1 (.) to Carney triad and others. In this chapter, we review all newly identified genetic associations and diseases associated with ACTs.整体 发表于 2025-3-22 16:23:09
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Genetics of Pheochromocytoma and Paraganglioma,spectively. Germline mutations can be identified in 40 % of patients with PCC/PGL with variable penetrance. There are at least 14 distinct germline susceptibility mutations implicated in the development of hereditary PCC/PGL and several additional somatic mutations involved in sporadic tumors. The g