Literature DB >> 11408759

Investigating familial endocrine neoplasia syndromes in children.

L B Johnston1, S L Chew, D Lowe, R Reznek, J P Monson, M O Savage.   

Abstract

Familial endocrine neoplasia syndromes multiple endocrine neoplasia (MEN) type 1, MEN type 2 and von Hippel Lindau (VHL) can now be diagnosed genetically in childhood. Paediatric endocrinologists must therefore be prepared to investigate and manage these children. This paper provides an overview of the major features of these syndromes and suggests protocols for regular screening of children known to be at risk of developing these disorders. Copyright 2001 S. Karger AG, Basel.

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Year:  2001        PMID： 11408759     DOI： 10.1159/000063460

Source DB:  PubMed          Journal:  Horm Res        ISSN： 0301-0163


  3 in total

Review 1.  Endocrine tumor syndromes in infancy and childhood.

Authors:  Ronald R de Krijger
Journal:  Endocr Pathol       Date:  2004       Impact factor: 3.943

2.  Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease.

Authors:  Astrid Rasmussen; Elisa Alonso; Adriana Ochoa; Irene De Biase; Itziar Familiar; Petra Yescas; Ana-Luisa Sosa; Yaneth Rodríguez; Mireya Chávez; Marisol López-López; Sanjay I Bidichandani
Journal:  BMC Med Genet       Date:  2010-01-12       Impact factor: 2.103

3.  Long-term follow-up and clinical course of a rare case of von Hippel-Lindau disease: A case report and review of the literature.

Authors:  Y U Zou; Jingjing Xu; Minming Zhang
Journal:  Oncol Lett       Date:  2016-03-29       Impact factor: 2.967
  3 in total

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