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GCK-MODY in a child with cystic fibrosis: the doubt of the treatment plan.

Authors :
Salzano, Giuseppina
Passanisi, Stefano
Lucanto, Maria Cristina
Costa, Stefano
Pajno, Giovanni Battista
Lombardo, Fortunato
Source :
Journal of Pediatric Endocrinology & Metabolism; Oct2020, Vol. 33 Issue 10, p1359-1362, 4p
Publication Year :
2020

Abstract

Objectives: The diagnosis of cystic fibrosis related diabetes (CFRD) is not often easy as glucose homeostasis may be influenced by various disease-related conditions such as enteral continuous drip feeding, frequent acute illness, use of systemic corticosteroids and other concomitant medications. Other forms of diabetes should be considered in the diagnostic work-up, particularly in the first decade of life. Case presentation: We hereby present the case of a cystic fibrosis 6-year-old female child diagnosed with glucokinase-maturity onset of diabetes of the young (GCK-MODY). The choice of treatment plan was doubtful since GCK-MODY does not usually require insulin treatment, but hyperglycemia could pose a threat to the respiratory tract. After intensive glucose monitoring, we decided to defer pharmacological treatment based on acceptable daily glycemic control. To date, no worsening in her respiratory function has been revealed. Conclusions: Recognition of non-CFRD forms of diabetes is fundamental to plan the most suitable treatment and follow-up. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0334018X
Volume :
33
Issue :
10
Database :
Supplemental Index
Journal :
Journal of Pediatric Endocrinology & Metabolism
Publication Type :
Academic Journal
Accession number :
146347013
Full Text :
https://doi.org/10.1515/jpem-2020-0093