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C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review
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). PATIEN...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794226/ https://www.ncbi.nlm.nih.gov/pubmed/36595822 http://dx.doi.org/10.1097/MD.0000000000032461 |
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author | Zhang, Di Chen, Congli Yang, Wenli Piao, Yurong Ren, Li Sang, Yanmei |
author_facet | Zhang, Di Chen, Congli Yang, Wenli Piao, Yurong Ren, Li Sang, Yanmei |
author_sort | Zhang, Di |
collection | PubMed |
description | 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). 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. 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. INTERVENTION: The patient was treated with fluid therapy, ketosis correction, insulin, and anti-infection treatment. OUTCOMES: After 17 days in the hospital, the blood glucose levels remained stable and the patient was discharged. 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. |
format | Online Article Text |
id | pubmed-9794226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-97942262022-12-28 C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review Zhang, Di Chen, Congli Yang, Wenli Piao, Yurong Ren, Li Sang, Yanmei Medicine (Baltimore) 4300 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). 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. 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. INTERVENTION: The patient was treated with fluid therapy, ketosis correction, insulin, and anti-infection treatment. OUTCOMES: After 17 days in the hospital, the blood glucose levels remained stable and the patient was discharged. 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. Lippincott Williams & Wilkins 2022-12-23 /pmc/articles/PMC9794226/ /pubmed/36595822 http://dx.doi.org/10.1097/MD.0000000000032461 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 4300 Zhang, Di Chen, Congli Yang, Wenli Piao, Yurong Ren, Li Sang, Yanmei C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review |
title | C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review |
title_full | C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review |
title_fullStr | C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review |
title_full_unstemmed | C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review |
title_short | C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review |
title_sort | c.487c>t mutation in pax4 gene causes mody9: a case report and literature review |
topic | 4300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794226/ https://www.ncbi.nlm.nih.gov/pubmed/36595822 http://dx.doi.org/10.1097/MD.0000000000032461 |
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