08 January 2021>: Articles
A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)
Rare disease
Natnicha Pongbangli A* , Kannika Pitipakorn B , Sasivimon Jai-aue B , Piyaporn Sirijanchune B , Sorawit Pongpittayut B , Wanwarang Wongcharoen EDOI: 10.12659/AJCR.928969
Am J Case Rep 2021; 22:e928969
Figure 1. The patient was characteristically prematurely aged, with short stature, and prominent eyes, a small chin, total alopecia, and protruding ears. The cutaneous findings of this patient demonstrated scleroderma-like skin changes and a loss of subcutaneous fat.