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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 E

DOI: 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.

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923