ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents

@article{Hattersley2018ISPADCP,
  title={ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents},
  author={A. Hattersley and S. Greeley and M. Polak and {\'O}. Rubio-Cabezas and P. Nj{\o}lstad and W. Młynarski and L. Castano and A. Carlsson and K. Raile and D. V. Ch{\'i} and S. Ellard and M. Craig},
  journal={Pediatric Diabetes},
  year={2018},
  volume={19},
  pages={47 - 63}
}
Monogenic diabetes results from one or more defects in a single gene. The disease may be inherited within families as a dominant, recessive or non-Mendelian trait or may present as a spontaneous case due to a de novo mutation (i.e. not inherited from parents). Well over 40 different genetic subtypes of monogenic diabetes have been identified to date, each having a typical phenotype and a specific pattern of inheritance. This article is protected by copyright. All rights reserved. 

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