Mody, the story of two siblings… the rare also happens!

Authors

  • Andreia Filipa Miranda Mota Department of Pediatrics, Hospital de São Bernardo, Centro Hospitalar de Setúbal
  • Susana Oliveira Parente Department of Pediatrics, Hospital de São Bernardo, Centro Hospitalar de Setúbal
  • José Oliveira Freixo Department of Pediatrics, Hospital de São Bernardo, Centro Hospitalar de Setúbal

DOI:

https://doi.org/10.25753/BirthGrowthMJ.v26.i3.9582

Keywords:

MODY, diabetes mellitus, mutation, GCK gene

Abstract

Maturity Onset Diabetes of the Young (MODY) defines a subtype of non-insulin diabetes mellitus, without insulin resistance or autoimmune pancreatic β-cell dysfunction. Affects 1-4% of paediatric patients with diabetes. Usually there is a family history and it starts before 25 years-old.
We present a clinical case of a previously healthy boy, who was diagnosed with type 1 diabetes mellitus due to fasting hyperglycaemia. After getting to know the MODY diagnosis in a not cohabitant sister from maternal lineage, we performed a genetic study which identified a heterozygote mutation in GCK gene.
The high clinical suspicion, usually supported by suggestive familiar history, is the first step to make the correct diagnosis. However, this uncommon form of diabetes and the need of expensive and long waiting complementary tests, delay identification, therapeutic and prognostic optimization, as well as genetic counselling.

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References

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Published

2017-09-05

How to Cite

1.
Mota AFM, Parente SO, Freixo JO. Mody, the story of two siblings… the rare also happens!. REVNEC [Internet]. 2017Sep.5 [cited 2024Mar.29];26(3):188-90. Available from: https://revistas.rcaap.pt/nascercrescer/article/view/9582

Issue

Section

Case Reports