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C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review.

Authors :
Zhang D
Chen C
Yang W
Piao Y
Ren L
Sang Y
Source :
Medicine [Medicine (Baltimore)] 2022 Dec 23; Vol. 101 (51), pp. e32461.
Publication Year :
2022

Abstract

Rationale: Maturity-onset diabetes of the young (MODY) is a group of autosomal dominant monogenic diabetes mellitus with a wide range of clinical manifestations that require distinct treatment strategies. MODY9 (OMIM # 612225) is a rare type of MODY, caused by a mutation in the Paired box gene 4 (PAX4).<br />Patient Concern: A 19-months boy was admitted to the department of endocrinology at Beijing Children's Hospital due to excessive water drinking, polyuria for over half a month, and wheezing for 3 days.<br />Diagnose: The whole-exon sequencing analysis demonstrated that the child carried the heterozygous missense mutation of c.487>T in the 7th exon region of PAX4 gene and diagnosed MODY9.<br />Intervention: The patient was treated with fluid therapy, ketosis correction, insulin, and anti-infection treatment.<br />Outcomes: After 17 days in the hospital, the blood glucose levels remained stable and the patient was discharged.<br />Lessons: In Chinese children, the heterozygous mutation of c.487C>T in the PAX4 gene can lead to the occurrence of MODY9.Gene sequencing analysis is of great significance in the diagnosis and classification of MODY.<br />Competing Interests: The authors have no conflicts of interest to disclose.<br /> (Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc.)

Details

Language :
English
ISSN :
1536-5964
Volume :
101
Issue :
51
Database :
MEDLINE
Journal :
Medicine
Publication Type :
Academic Journal
Accession number :
36595822
Full Text :
https://doi.org/10.1097/MD.0000000000032461