The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome.
In: Annals of Pediatric Endocrinology & Metabolism, Jg. 29 (2024-02-01), Heft 1, S. 70-72
Online
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Zugriff:
This article reports on the first case of hyperosmolar diabetic ketoacidosis (HODKA) in a 12-year-old girl diagnosed with maturity-onset diabetes of the young type 5 (MODY 5) and 17q12 microdeletion syndrome. The patient presented with hyperglycemic symptoms and was initially diagnosed with type 1 diabetes mellitus. She experienced acute complications such as thrombocytopenia-associated multiple organ failure, cerebral microbleeds, and diabetic amyotrophy. The article highlights the importance of identifying hyperosmolarity in HODKA and emphasizes the need for aggressive fluid administration in its treatment. [Extracted from the article]
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The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome.
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Autor/in / Beteiligte Person: | Lee, Jun ; Kim, Minji ; Yoo, Sukdong ; Ju Young Yoon ; Chong Kun Cheon |
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Zeitschrift: | Annals of Pediatric Endocrinology & Metabolism, Jg. 29 (2024-02-01), Heft 1, S. 70-72 |
Veröffentlichung: | 2024 |
Medientyp: | academicJournal |
ISSN: | 2287-1012 (print) |
DOI: | 10.6065/apem.2346006.003 |
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