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Endocrine Manifestations of Von Hippel-Landau Disease.
Pradhan, Roma; George, Nelson; Mandal, Kaushik; Agarwal, Amit; Gupta, Sushil K.
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  • Pradhan R; Department of Endocrine Surgery, Dr. RMLIMS, Lucknow, Uttar Pradesh, India.
  • George N; Department of Endocrine Surgery, SGPGIMS, Lucknow, Uttar Pradesh, India.
  • Mandal K; Department of Genetics, SGPGIMS, Lucknow, Uttar Pradesh, India.
  • Agarwal A; Department of Endocrine Surgery, SGPGIMS, Lucknow, Uttar Pradesh, India.
  • Gupta SK; Department of Endocrinology, SGPGIMS, Lucknow, Uttar Pradesh, India.
Indian J Endocrinol Metab ; 23(1): 159-164, 2019.
Article en En | MEDLINE | ID: mdl-31016171
Von Hippel-Lindau (VHL) disease is an autosomal dominant disorder characterized by various endocrine, nonendocrine, benign, and malignant tumors in various organs. VHL tumor suppressor gene, located on short arm of chromosome 3 is responsible for this. Pheochromocytoma (PCC) is one of the important endocrine manifestations that needs to be ruled out in case of VHL suspicion. In this review, we summarize the endocrine manifestations of VHL disease and their management while giving case history of five such cases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Indian J Endocrinol Metab Año: 2019 Tipo del documento: Article País de afiliación: India Pais de publicación: India
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Indian J Endocrinol Metab Año: 2019 Tipo del documento: Article País de afiliación: India Pais de publicación: India