Non-MEN Familial Endocrine Syndromes: Von Recklinghausen Disease, Von Hippel-Lindau Syndrome, Pheochromocytoma/Paraganglioma

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dc.authorscopusid36089061500
dc.authorscopusid8368936600
dc.contributor.authorAgcaoglu, O.
dc.contributor.authorMakay, Ö.
dc.date.accessioned2024-08-25T18:51:58Z
dc.date.available2024-08-25T18:51:58Z
dc.date.issued2022
dc.departmentEge Üniversitesien_US
dc.description.abstractThis chapter briefly describes familial endocrine syndromes besides MEN, including hereditary pheochromocytoma or paragangliomas, von Hippel-Lindau syndrome, and neurofibromatosis type 1 (von Recklinghausen disease). The contents of this chapter include a summary of the most recent literature regarding the epidemiology and genetics, clinical presentations, diagnosis and indications for surgery, preoperative management and radiological studies, surgical techniques and approaches, postoperative follow-up, and prognosis for these syndromes. © Springer Nature Switzerland AG 2021.en_US
dc.identifier.doi10.1007/978-3-030-84737-1_39
dc.identifier.endpage968en_US
dc.identifier.isbn9783030847371
dc.identifier.isbn9783030847364
dc.identifier.scopus2-s2.0-85174763195en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage951en_US
dc.identifier.urihttps://doi.org/10.1007/978-3-030-84737-1_39
dc.identifier.urihttps://hdl.handle.net/11454/102789
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherSpringer International Publishingen_US
dc.relation.ispartofEndocrine Surgery Comprehensive Board Exam Guideen_US
dc.relation.publicationcategoryKitap Bölümü - Uluslararasıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmz20240825_Gen_US
dc.subjectAdrenalectomyen_US
dc.subjectEndocrine surgeryen_US
dc.subjectFamilial endocrine syndromesen_US
dc.subjectNeurofibromatosis type 1en_US
dc.subjectParagangliomaen_US
dc.subjectPheochromocytomaen_US
dc.subjectVon Hippel-Lindau syndromeen_US
dc.subjectVon Recklinghausen diseaseen_US
dc.titleNon-MEN Familial Endocrine Syndromes: Von Recklinghausen Disease, Von Hippel-Lindau Syndrome, Pheochromocytoma/Paragangliomaen_US
dc.typeBook Chapteren_US

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