Case Report of a Patient with Mauriac Syndrome
Suprianto Suryono, Muhammad Umer Malik, Chee Kwang Yung, Edwin Lim Chyi Chyuan, Pg Adli Pg Metussin
Asian Journal of Case Reports in Medicine and Health · pp. 37–43 · Published 30 Mar 2021
Abstract
We would like to present an interesting and rare case of a 16-year boy, with the background of Type 1 diabetes since the age of 11 years who presented with Diabetic Ketoacidosis (DKA). He had multiple admissions with DKA in the preceding two years and his liver function tests were found to be deranged during the last two presentations. This was further evaluated through various investigations and a diagnosis of Mauriac syndrome was made.
Cited by 0
No indexed citations yet.
Related research
- Successful Treatment of Pulmonary Embolus Secondary to Diabetic Ketoacidosis with Tissue Plasminogen Activator — shares topic coverage
- Study of QTc Interval Prolongation in Diagnosed Cases of Diabetic Ketoacidosis with Reference to Electrolyte Imbalances — shares topic coverage
- Glycemic Control Strategies and Management of Acute Complications in Children with Type 1 Diabetes: A Systematic Review — shares topic coverage
- Persistent Complete Heart Block Unmasked by Severe Diabetic Ketoacidosis in a Young Woman: A Case Report — shares topic coverage
- Treatment of Chronic and Severe Diabetes Mellitus with Ketoacidosis in a Four-Year-Old Intact Female American Pit Bull Terrier — shares topic coverage
Article metrics
Real usage data collected on this platform.
0
Page views
0
PDF downloads
0
Outbound clicks
0
Citations
Views by country
Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".
No views recorded yet.
Traffic sources
Referring site, by host.
No traffic recorded yet.
Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.