Article
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 - 27 Oct 2020
Majumder Sananda, Chakraborty Partha Pratim, Ghosh Prakash Chandra, Bera Mitali
Abstract excerpt
Endogenous Cushing's syndrome (CS) is rare in infancy. Bilateral micronodular adrenocortical disease (BMAD), either primary pigmented nodular adrenocortical disease or the non-pigmented isolated micronodular adrenocortical disease is an important aetiology of CS in this age group, which requires bilateral adrenalectomy for cure. BMAD may be isolated, or a component of Carney complex. Isolated sporadic BMAD...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
