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  • Cushing’s syndrome in early infancy due to isolated sporadic bilateral micronodular adrenocortical disease associated with myosin heavy chain 8 mutation: diagnostic challenges, too many!

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Unusual association of diseases/symptoms
Case report
Cushing’s syndrome in early infancy due to isolated sporadic bilateral micronodular adrenocortical disease associated with myosin heavy chain 8 mutation: diagnostic challenges, too many!

Authors

  1. Correspondence to Partha Pratim Chakraborty; docparthapc{at}yahoo.co.in
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Citation

Majumder S, Chakraborty PP, Ghosh PC, et al
Cushing’s syndrome in early infancy due to isolated sporadic bilateral micronodular adrenocortical disease associated with myosin heavy chain 8 mutation: diagnostic challenges, too many!
BMJ Case Reports CP 2020;13:e236850.

Publication history

  • Accepted October 4, 2020
  • First published October 27, 2020.
Online issue publication 
March 23, 2021

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© BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.