Keimyung University Dongsan Hospital Researchers Describe Findings in Pediatrics (A Case of Chromosome 17q12 Deletion Syndrome with Type 2 Mayer-Rokitansky-Kuster-Hauser Syndrome and Maturity-Onset Diabetes of the Young Type 5).
In: Diabetes Week, 2024-05-13, S. 109-109
serialPeriodical
Zugriff:
A recent report from Keimyung University Dongsan Hospital in South Korea describes a case of chromosome 17q12 deletion syndrome, a rare genetic disorder. The patient, a 14-year-old Korean female, exhibited a range of symptoms including maturity-onset diabetes of the young type 5 (MODY5), Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, developmental delay, kidney abnormalities, and more. The management of this complex condition required a comprehensive and multidisciplinary approach, including insulin injections, gynecological evaluation, and tailored interventions across various medical specialties. The research emphasizes the importance of regular monitoring, individualized care, and psychosocial support for individuals with chromosome 17q12 deletion syndrome. [Extracted from the article]
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Titel: |
Keimyung University Dongsan Hospital Researchers Describe Findings in Pediatrics (A Case of Chromosome 17q12 Deletion Syndrome with Type 2 Mayer-Rokitansky-Kuster-Hauser Syndrome and Maturity-Onset Diabetes of the Young Type 5).
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Zeitschrift: | Diabetes Week, 2024-05-13, S. 109-109 |
Veröffentlichung: | 2024 |
Medientyp: | serialPeriodical |
ISSN: | 1537-1425 (print) |
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